MP:0000033 | absent cochlear duct | "missing spiral tube within the cochlea; contains the neuroepithelial receptor organ for hearing" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:23837] |
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Allelic Composition: Mdm2tm1Bay/Mdm2tm1Bay,Trp53tm1Snj/Trp53tm1Snj Genetic Background: involves: C57BL/6
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MP:0000041 | absent endolymphatic duct | "missing small membranous canal of the inner ear; connecting membranous labyrinth with the endolymphatic sac" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:1776] |
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Allelic Composition: Mdm2tm1Bay/Mdm2tm1Bay,Trp53tm1Snj/Trp53tm1Snj Genetic Background: involves: C57BL/6
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MP:0000074 | abnormal neurocranium morphology | "malformed bones of the skull enclosing the brain" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:55583] |
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Allelic Composition: ShhDsh/Shh+ Genetic Background: B10Rl.Cg-ShhDsh
Allelic Composition: Ccd/Ccd+,ShhDsh/Shh+ Genetic Background: involves: 101 * C3H * C57BL * C57BL/10Rl * SEC
Allelic Composition: Shhtm2Chg/Shh+,Edil3Tg(Sox2-cre)1Amc/Edil3+ Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA
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MP:0000077 | abnormal interparietal bone morphology | "malformed bone of the cranium; lies above and anterior to the occipital bone " [J:61509] |
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Allelic Composition: Ccd/Ccd+,ShhDsh/Shh+ Genetic Background: involves: 101 * C3H * C57BL * C57BL/10Rl * SEC
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MP:0000087 | absent mandible | "missing the lower bony framework of the mouth where the inferior teeth are held" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
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Allelic Composition: Shhtm1Chg/Shh+,Sulf1Gt(XM190)Byg/Sulf1Gt(XM190)Byg,Sulf2Gt(PST111)Byg/Sulf2Gt(PST111)Byg Genetic Background: involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/10
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MP:0000088 | short mandible | "reduced length of the lower bony framework of the mouth where the inferior teeth are held" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator] |
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Allelic Composition: Gas1tm2Fan/Gas1tm2Fan,Shhtm1Chg/Shh+ Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6J
Allelic Composition: Shhtm1Chg/Shh+,Sulf1Gt(XM190)Byg/Sulf1Gt(XM190)Byg,Sulf2Gt(PST111)Byg/Sulf2Gt(PST111)Byg Genetic Background: involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/10
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MP:0000090 | absent premaxilla | "missing anterior and interior portion of the maxilla" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:17489] |
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Allelic Composition: Disp1tm2Amc/Disp1tm2Amc Genetic Background: involves: 129/Sv * C57BL/6J * SWR
Allelic Composition: Disp1icb/Disp1tm2Amc,Shhtm1(EGFP/cre)Cjt/Shh+ Genetic Background: involves: 129/Sv * C57BL/6J * SWR
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MP:0000094 | absent alveolar process | "missing projecting ridge on the inferior surface of the body of the maxilla containing the tooth sockets" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:17489] |
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Allelic Composition: Shhtm1Amc/Shhtm2Amc,Tg(KRT14-cre)1Amc/0 Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA
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MP:0000102 | abnormal nasal bone morphology | "malformed elongated rectangular bone that forms part of the nasal bridge" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:17489] |
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Allelic Composition: Shhtm1Amc/Shhtm2Amc,Tg(KRT14-cre)1Amc/0 Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA
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MP:0000107 | abnormal frontal bone morphology | "malformed bone forming the forehead and part of the eye orbit" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:17489] |
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Allelic Composition: ShhDsh/Shh+ Genetic Background: B10Rl.Cg-ShhDsh
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MP:0000109 | abnormal parietal bone morphology | "malformed curved bone forming part of the vault of the cranium" [J:17489] |
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Allelic Composition: Disp1tm2Amc/Disp1tm2Amc Genetic Background: involves: 129/Sv * C57BL/6J * SWR
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MP:0000118 | arrest of tooth development | "failure of differentiation of the teeth" [J:18378] |
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Allelic Composition: Shhtm1Amc/Shhtm2Amc,Tg(KRT14-cre)1Amc/0 Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA
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MP:0000128 | growth retardation of molars | "developmental delay of the growth of the molars" [J:17489] |
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Allelic Composition: Shhtm1Amc/Shhtm2Amc,Tg(KRT14-cre)1Amc/0 Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA
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MP:0000137 | abnormal vertebrae morphology | "malformed bony segment of the spinal column" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8] |
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Allelic Composition: Irs2tm1Mfw/Irs2tm1Mfw Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6J
Allelic Composition: Ccd/Ccd+,ShhDsh/Shh+ Genetic Background: involves: 101 * C3H * C57BL * C57BL/10Rl * SEC
Allelic Composition: Shhtm1Amc/Shhtm1Amc Genetic Background: involves: 129S1/Sv * 129X1/SvJ
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MP:0000138 | absent vertebrae | "missing bony segments of the spinal column" [J:35802] |
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Allelic Composition: Fgfr2tm1.1Dsn/Fgfr2+ Genetic Background: involves: 129P2/OlaHsd * C57BL/6
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MP:0000141 | abnormal vertebral body morphology | "malformed main portion of the vertebra anterior to the vertebral canal" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:55583] |
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Allelic Composition: Gas1tm2Fan/Gas1tm2Fan,Shhtm1Chg/Shh+ Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6J
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MP:0000149 | abnormal scapula morphology | "malformation of either or both of the large, flat bones of the back part of the shoulder" [J:13049] |
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Allelic Composition: Ccd/Ccd+,ShhDsh/Shh+ Genetic Background: involves: 101 * C3H * C57BL * C57BL/10Rl * SEC
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MP:0000150 | abnormal rib morphology | "malformed bones forming the bony wall of the chest" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, J:50311] |
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Allelic Composition: Irs2tm1Mfw/Irs2tm1Mfw Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6J
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MP:0000159 | abnormal xiphoid process | "malformed posterior tip of the sternum" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, J:42932] |
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Allelic Composition: Ccd/Ccd+,ShhDsh/Shh+ Genetic Background: involves: 101 * C3H * C57BL * C57BL/10Rl * SEC
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MP:0000163 | abnormal cartilage morphology | "anomalous structure or development of the nonvascular, resilient, flexible connective tissue found primarily in joints, walls of the throax, and tubular structures, but which also comprises most of the skeleton in early fetal life " [Stedman s Medical Dictionary:ISBN 0-683-40008-8] |
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Allelic Composition: Irs2tm1Mfw/Irs2tm1Mfw Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6J
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MP:0000164 | abnormal cartilage development | "anomalous formation of the nonvascular, resilient, flexible connective tissue found primarily in joints, walls of the throax, and tubular structures, but which also comprises most of the skeleton in early fetal life " [Stedman s Medical Dictionary:ISBN 0-683-40008-8] |
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Allelic Composition: Irs2tm1Mfw/Irs2tm1Mfw Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6J
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MP:0000266 | abnormal cardiac morphology | "anomalies in the hollow, muscular organ that maintains the circulation of the blood" [MeSH:National Library of Medicine - Medical Subject Headings , 2003] |
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Allelic Composition: Fgfr2tm1.1Dsn/Fgfr2+ Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Allelic Composition: Shhtm1Chg/Shhtm1Chg,Zic2Ku/Zic2Ku Genetic Background: involves: 129S1/Sv * 129X1/SvJ * BALB/cAnNCrl * C3H/HeH
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MP:0000270 | abnormal heart tube morphology | "malformed embryonic heart " [J:37888] |
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Allelic Composition: Gas1tm2Fan/Gas1tm2Fan,Shhtm1Chg/Shhtm1Chg Genetic Background: involves: 129/Sv * 129S1/Sv * 129X1/SvJ * C57BL/6J
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MP:0000291 | enlarged pericardium | "extended fibroserous membrane covering the heart and beginning of the great vessels" [J:29971] |
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Allelic Composition: Gas1tm2Fan/Gas1tm2Fan,Shhtm1Chg/Shhtm1Chg Genetic Background: involves: 129/Sv * 129S1/Sv * 129X1/SvJ * C57BL/6J
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MP:0000352 | decreased cell proliferation | "less than the normal growth and reproduction of similar cells" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator] |
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Allelic Composition: Gt(ROSA)26Sortm1(tetO-Sox9)Msan/Gt(ROSA)26Sor+,Tg(SFTPC-rtTA)5Jaw/0 Genetic Background: Not Specified
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MP:0000377 | abnormal hair follicle | "malformed invagination of the epidermis from which the hair shaft develops" [J:65031] |
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Allelic Composition: Irx4tm1Jse/Irx4+ Genetic Background: involves: 129X1/SvJ * Black Swiss
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MP:0000378 | absent hair follicles | "missing epidermal invaginations from which the hair shaft develops" [J:65039] |
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Allelic Composition: Shhtm1Amc/Shhtm1Amc Genetic Background: involves: 129/Sv * C57BL/6J * CBA/J
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MP:0000383 | abnormal hair follicle orientation | "misaligned hair follicles; hair follicles that do not orient in a typical pattern" [J:47620] |
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Allelic Composition: Irx4tm1Jse/Irx4+ Genetic Background: involves: 129X1/SvJ * Black Swiss
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MP:0000388 | absent inner root sheath | "missing epidermally derived layer surrounding the hair follicle; innermost of two layers" [J:65047] |
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Allelic Composition: Shhtm1Amc/Shhtm1Amc Genetic Background: involves: 129/Sv * C57BL/6J * CBA/J
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MP:0000413 | polyphalangy | "increased number of phalanges in any of the digits" [J:13069, csmith:Cynthia L. Smith, Mouse Genome Informatics Curator] |
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Allelic Composition: Gt(ROSA)26Sortm1(Grem1)Svok/Gt(ROSA)26Sor+,Shhtm1(EGFP/cre)Cjt/0 Genetic Background: involves: 129S1/Sv
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MP:0000414 | alopecia | "absence of hair or loss of hair; not usually in reference to primary genetic hairlessness but may be due to dietary, stress, secondary to immune condition" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, J:30772, J:33796] |
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Allelic Composition: Irx4tm1Jse/Irx4+ Genetic Background: involves: 129X1/SvJ * Black Swiss
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MP:0000428 | abnormal craniofacial morphology | "anomalous structure or development of the face and/or cranium" [Stedman s Medical Dictionary:ISBN 0-683-40008-8] |
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Allelic Composition: Fgfr2tm1.1Dsn/Fgfr2+ Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Allelic Composition: Gas1tm2Fan/Gas1tm2Fan,Shhtm1Chg/Shh+ Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6J
Allelic Composition: Shhtm1Amc/Shhtm2Amc,Tg(Thy1-cre)703Vaw/? Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C3H * C57BL/6
Allelic Composition: Shhtm1Chg/Shh+,Sulf1Gt(XM190)Byg/Sulf1Gt(XM190)Byg,Sulf2Gt(PST111)Byg/Sulf2Gt(PST111)Byg Genetic Background: involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/10
Allelic Composition: HhatTg(TFAP2A-cre)1Will/Hhat+,Shhtm1Chg/Shh+ Genetic Background: involves: 129S1/Sv * 129X1/SvJ
Allelic Composition: Shhtm3(cre)Chg/Shhtm3(cre)Chg Genetic Background: Not Specified
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MP:0000433 | microcephaly | "an abnormally small head" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
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Allelic Composition: ShhDsh/Shh+ Genetic Background: B10Rl.Cg-ShhDsh
Allelic Composition: Shhtm2Amc/Shhtm2Amc,Tg(Nes-cre)1Kln/0 Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL
Allelic Composition: Shhtm1Amc/Shhtm2Amc,Tg(Thy1-cre)703Vaw/? Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C3H * C57BL/6
Allelic Composition: Six3tm3.1Gco/Six3+,Shhtm1Chg/Shh+ Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
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MP:0000434 | megacephaly | "an abnormally large size of the head" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
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Allelic Composition: Gli2tm2.1Alj/Gli2+,Shhtm1Chg/Shhtm1Chg Genetic Background: either: (involves: 129) or (involves: 129 * Black Swiss)
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MP:0000438 | abnormal skull morphology | "anomalous structure or development of the cranium" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator] |
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Allelic Composition: Irs2tm1Mfw/Irs2tm1Mfw Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6J
Allelic Composition: Ccd/Ccd+,ShhDsh/Shh+ Genetic Background: involves: 101 * C3H * C57BL * C57BL/10Rl * SEC
Allelic Composition: Shhtm1Amc/Shhtm2Amc,Tg(KRT14-cre)1Amc/0 Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA
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MP:0000445 | short snout | "reduced length of the anterior facial part of the muzzle" [J:53370] |
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Allelic Composition: Shhtm1Chg/Shh+,Vps25m1Lis/Vps25m1Lis Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C3H * C57BL/6J
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MP:0000453 | absent mouth | "missing oral cavity" [J:35802] |
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Allelic Composition: ShhDsh/Shh+ Genetic Background: B10Rl.Cg-ShhDsh
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MP:0000455 | abnormal maxilla morphology | "malformation of the upper bony framework of the mouth where the superior teeth are held" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8] |
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Allelic Composition: Irs2tm1Mfw/Irs2tm1Mfw Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6J
Allelic Composition: Ccd/Ccd+,ShhDsh/Shh+ Genetic Background: involves: 101 * C3H * C57BL * C57BL/10Rl * SEC
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MP:0000460 | mandible hypoplasia | "arrested growth or atrophy of the lower bony framework of the mouth where the inferior teeth are held" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, tc:Teresa Chu , Mouse Genome Informatics Curator, J:54637] |
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Allelic Composition: Chd7Whi/Chd7+ Genetic Background: C3HeB/FeJ-Chd7Whi
Allelic Composition: Shhtm1Chg/Shh+,Vps25m1Lis/Vps25m1Lis Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C3H * C57BL/6J
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MP:0000462 | abnormal digestive system morphology | "anomalous structure of the system dedicated to the mechanical, chemical, and enzymatic processing of food" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator, Stedman s Medical Dictionary:ISBN 0-683-40008-8] |
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Allelic Composition: Irx4tm1Jse/Irx4+ Genetic Background: involves: 129X1/SvJ * Black Swiss
Allelic Composition: Shhtm3(cre)Chg/Shhtm3(cre)Chg Genetic Background: Not Specified
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MP:0000467 | abnormal esophagus morphology | "malformation of the part of the digestive canal through which food passes from the pharynx to the stomach" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, MGI:tc] |
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Allelic Composition: Irx4tm1Jse/Irx4+ Genetic Background: involves: 129X1/SvJ * Black Swiss
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MP:0000468 | abnormal esophageal epithelium morphology | "malformation of the epithelial layer of the esophagus" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, MGI:tc] |
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Allelic Composition: Jag1Yo/Jag1Yo Genetic Background: C3HeB/FeJ-Jag1Yo
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MP:0000473 | abnormal stomach glandular epithelium morphology | "malformation of the gland-containing epithelial layer of the stomach" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, MGI:tc, J:54637] |
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Allelic Composition: Shhtm1Amc/Shhtm1Amc Genetic Background: involves: 129/Sv * C57BL/6J * CBA/J
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MP:0000474 | abnormal foregut morphology | "malformed cephalic portion of the primitive digestive tube of the embryo" [J:35802] |
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Allelic Composition: Fgfr2tm1.1Dsn/Fgfr2+ Genetic Background: involves: 129P2/OlaHsd * C57BL/6
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MP:0000484 | abnormal pulmonary artery morphology | "structrual anomaly of the artery that arises from the right ventricle and conveys unaerated blood to the lungs " [MeSH:National Library of Medicine - Medical Subject Headings, 2003, hdene:Howard Dene, Mouse Genome Informatics Curator] |
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Allelic Composition: Lamp1tm1Psa/Lamp1tm1Psa,Lamp2tm1Psa/Y Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Allelic Composition: Ctnnb1tm1Mmt/Ctnnb1tm1Mmt,Shhtm1(EGFP/cre)Cjt/Shh+ Genetic Background: involves: 129X1/SvJ
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MP:0000495 | abnormal colon morphology | "malformation of the portion of the large intestine between the cecum and the rectum" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
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Allelic Composition: Shhtm1Amc/Shhtm1Amc Genetic Background: involves: 129/Sv * C57BL/6J * CBA/J
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MP:0000496 | abnormal small intestine morphology | "structural or developmental anomalies of the intestinum tenue " [Stedman s Medical Dictionary:ISBN 0-683-40008-8] |
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Allelic Composition: Irx4tm1Jse/Irx4+ Genetic Background: involves: 129X1/SvJ * Black Swiss
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MP:0000519 | hydronephrosis | "dilation of the pelvis and calices of one or both kidneys" [J:56641] |
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Allelic Composition: Smn1tm5(Smn1/SMN2)Mrph/Smn1tm5(Smn1/SMN2)Mrph Genetic Background: FVB.129(B6)-Smn1tm5(Smn1/SMN2)Mrph/J
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MP:0000536 | hydroureter | "distention of the ureter with urine, due to blockage from any cause" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, MGI:Cml, J:13044] |
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Allelic Composition: Smn1tm5(Smn1/SMN2)Mrph/Smn1tm5(Smn1/SMN2)Mrph Genetic Background: FVB.129(B6)-Smn1tm5(Smn1/SMN2)Mrph/J
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MP:0000547 | short limbs | "reduced average length of the extremities" [MGI:CLS, J:61509] |
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Allelic Composition: ShhDsh/ShhDsh Genetic Background: involves: 101 * C3H * C57BL * SEC
Allelic Composition: ShhDsh/ShhDsh Genetic Background: B10Rl.Cg-ShhDsh
Allelic Composition: Shhtm1Chg/Shhtm1Chg Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
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MP:0000551 | absent forelimb | "missing the entire anterior extremities" [MGI:tc, J:54637] |
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Allelic Composition: Fgfr2tm1.1Dsn/Fgfr2+ Genetic Background: involves: 129P2/OlaHsd * C57BL/6
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MP:0000554 | abnormal carpal bone morphology | "malformation of the nine nodular bones of the joint between the forelimb bones and the front paws consisting of the scapholunar, triangular, greater multiangular, lesser multiangular, capitate, hamate, centrale and the sesamoids" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, Anatomy of the Rat:Greene, EC, Hafner Publishing Co, 1935] |
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Allelic Composition: Cd19tm1(cre)Cgn/Cd19+,Gt(ROSA)26Sortm4(Ikbkb)Rsky/Gt(ROSA)26Sor+ Genetic Background: involves: 129P2/OlaHsd * C57BL/6
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MP:0000556 | abnormal hindlimb morphology | "malformation of the entire posterior extremities" [MGI:tc] |
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Allelic Composition: ShhDsh/Shh+ Genetic Background: B10Rl.Cg-ShhDsh
Allelic Composition: Ccd/Ccd+,ShhDsh/Shh+ Genetic Background: involves: 101 * C3H * C57BL * C57BL/10Rl * SEC
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MP:0000557 | absent hindlimb | "missing the entire posterior extremities" [MGI:tc, J:54637] |
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Allelic Composition: Fgfr2tm1.1Dsn/Fgfr2+ Genetic Background: involves: 129P2/OlaHsd * C57BL/6
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MP:0000561 | adactyly | "missing all digits; usually refered to as a congenital condition" [tc:Teresa Chu , Mouse Genome Informatics Curator, J:54637] |
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Allelic Composition: Fgfr2tm1.1Dsn/Fgfr2+ Genetic Background: involves: 129P2/OlaHsd * C57BL/6
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MP:0000562 | polydactyly | "greater than 5 digits on one or more autopods" [Stedman s Medical Dictionary:ISBN 0-683-40008-8] |
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Allelic Composition: Cd19tm1(cre)Cgn/Cd19+,Gt(ROSA)26Sortm4(Ikbkb)Rsky/Gt(ROSA)26Sor+ Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Allelic Composition: Gli3tm2Blnw/Gli3+,Shhtm1Chg/Shhtm1Chg Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N
Allelic Composition: ShhM101116/Shh+ Genetic Background: D2;B6-ShhM101116/Rbrc
Allelic Composition: ShhM101116/ShhM101116 Genetic Background: D2;B6-ShhM101116/Rbrc
Allelic Composition: ShhDz/ShhDz Genetic Background: C57BL/6J-ShhDz
Allelic Composition: ShhDz/Shh+ Genetic Background: C57BL/6J-ShhDz
Allelic Composition: Shhtm1Chg/Shh+,Vps25m1Lis/Vps25m1Lis Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C3H * C57BL/6J
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MP:0000564 | syndactyly | "any degree of webbing or fusion of the digits, may involve only soft tissues or also can include bone" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8] |
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Allelic Composition: ShhDsh/Shh+ Genetic Background: B10Rl.Cg-ShhDsh
Allelic Composition: Ccd/Ccd+,ShhDsh/Shh+ Genetic Background: involves: 101 * C3H * C57BL * C57BL/10Rl * SEC
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MP:0000565 | oligodactyly | "congenital condition in which some digits or parts of digits are missing" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:53370] |
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Allelic Composition: Hhattm2Ptch/Hhattm2Ptch Genetic Background: involves: 129P2/OlaHsd * FVB/N * various
Allelic Composition: Disp1icb/Disp1tm1Amc,Shhtm1(EGFP/cre)Cjt/Shh+ Genetic Background: involves: 129X1/SvJ * C57BL/6J
Allelic Composition: Fgfr1tm3.2Cxd/Fgfr1tm3.2Cxd,Shhtm1(EGFP/cre)Cjt/Shh+ Genetic Background: involves: 129S6/SvEvTac
Allelic Composition: Fgfr1tm3.1Cxd/Fgfr1tm3.2Cxd,Shhtm1(EGFP/cre)Cjt/Shh+ Genetic Background: involves: 129S6/SvEvTac
Allelic Composition: Gas1tm2Fan/Gas1tm2Fan,Shhtm1Chg/Shh+ Genetic Background: involves: 129/Sv * 129S1/Sv * 129X1/SvJ * C57BL/6J
Allelic Composition: Gas1tm2Fan/Gas1tm2Fan,Shhtm1Chg/Shh+ Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6J
Allelic Composition: Shhtm1Chg/Shhtm1Chg,Tulp3hhkr/Tulp3hhkr Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C3H/HeH * C57BL/6
Allelic Composition: Shhtm1Chg/Shhtm1Chg,Tmem107schlei/Tmem107schlei Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C3HeB/FeJ * C57BL/6J
Allelic Composition: Gata6tm2.1Sad/Gata6tm2.1Sad,Shhtm2Amc/Shhtm2Amc,Tg(Prrx1-cre)1Cjt/0 Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * SJL/J
Allelic Composition: Rr29tm1.1Bobh/Rr29+,Shhtm1Chg/Shh+ Genetic Background: involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ
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MP:0000566 | synostosis | "osseous union of two bones that are not normally connected" [J:13049] |
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Allelic Composition: Gli3tm2Blnw/Gli3+,Shhtm1Chg/Shhtm1Chg Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N
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MP:0000572 | abnormal autopod morphology | "malformation of the hand or foot" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator] |
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Allelic Composition: Gli3tm2Blnw/Gli3+,Shhtm1Chg/Shhtm1Chg Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N
Allelic Composition: Shhtm1Chg/Shhtm1Chg Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
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MP:0000596 | abnormal liver development | "anomalous differentiation of the liver" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator] |
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Allelic Composition: Lamp1tm1Psa/Lamp1tm1Psa,Lamp2tm1Psa/Y Genetic Background: involves: 129P2/OlaHsd * C57BL/6
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MP:0000639 | abnormal adrenal gland morphology | "malformed endocrine glands located above the kidney responsible for hormone and epinephrine secretion" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:61190] |
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Allelic Composition: Edardl-J/Edardl-J Genetic Background: involves: C3HeB/FeJ
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MP:0000646 | enlarged adrenocortical cells | "larger size of cells of the adrenal gland " [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:54931] |
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Allelic Composition: Edardl-J/Edardl-J Genetic Background: involves: C3HeB/FeJ
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MP:0000755 | hindlimb paralysis | "loss of power of voluntary movement in the muscles of the hindlimb through injury or disease of it or its nerve supply" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8] |
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Allelic Composition: Shhtm1Ahk/Shhtm1Ahk,Slc6a3tm1(cre)Xz/Slc6a3+ Genetic Background: involves: 129S1/Sv * C57BL/6
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MP:0000767 | abnormal smooth muscle morphology | "anomalous structure of any of the unstriated muscle fibers of the internal organs, blood vessels, hair follicles, etc. " [Stedman s Medical Dictionary:ISBN 0-683-40008-8] |
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Allelic Composition: Irx4tm1Jse/Irx4+ Genetic Background: involves: 129X1/SvJ * Black Swiss
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MP:0000774 | reduced brain size | "smaller appearance of the brain" [J:35802] |
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Allelic Composition: Fgfr2tm1.1Dsn/Fgfr2+ Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Allelic Composition: Shhtm2Amc/Shhtm2Amc,Tg(Nes-cre)1Kln/0 Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL
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MP:0000780 | abnormal corpus callosum morphology | "malformation or absence of a thick bundle of nerve fibers comprising a commissural plate connecting the two cerebral hemispheres; it consists of contralateral axon projections that provides communications between the right and left cerebral hemispheres" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
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Allelic Composition: Shhtm2Chg/Shh+,Edil3Tg(Sox2-cre)1Amc/Edil3+ Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA
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MP:0000783 | abnormal forebrain morphology | "malformed or absent anterior primitive cerebral vesicle; most rostral of three primary vesicles of the embryonic neural tube" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:38857] |
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Allelic Composition: Fgfr2tm1.1Dsn/Fgfr2+ Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Allelic Composition: Ndst1tm1.1Grob/Ndst1tm1.1Grob,Shhtm1Chg/Shh+ Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Allelic Composition: Shhtm1Chg/Shhtm1Chg,Zic2Ku/Zic2Ku Genetic Background: involves: 129S1/Sv * 129X1/SvJ * BALB/cAnNCrl * C3H/HeH
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MP:0000787 | abnormal telencephalon morphology | "any malformation or absence of the paired anteriolateral division of the prosencephalon plus the lamina terminalis from which the olfactory lobes, cerebral cortex, and subcortical nuclei are derived " [MeSH:National Library of Medicine - Medical Subject Headings , 2003, Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8] |
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Allelic Composition: Fgfr2tm1.1Dsn/Fgfr2+ Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Allelic Composition: Shhtm2Chg/Shh+,Edil3Tg(Sox2-cre)1Amc/Edil3+ Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA
Allelic Composition: Six3tm3.1Gco/Six3+,Shhtm1Chg/Shh+ Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
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MP:0000808 | abnormal hippocampus development | "improper differentiation of the hippocampus" [tc:Teresa Chu , Mouse Genome Informatics Curator] |
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Allelic Composition: Shhtm2Chg/Shh+,Edil3Tg(Sox2-cre)1Amc/Edil3+ Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA
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MP:0000820 | abnormal choroid plexus morphology | "malformed or absent fringe of the tela choroidea of the cerebral ventricles" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:45302] |
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Allelic Composition: Shhtm2Chg/Shh+,Edil3Tg(Sox2-cre)1Amc/Edil3+ Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA
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MP:0000830 | abnormal diencephalon morphology | "any malformation or absence of the paired caudal parts of the prosencephalon from which the thalamus, hypothalamus, epithalamus and subthalamus are derived; these regions regulate autonomic, visceral and endocrine function, and process information directed to the cerebral cortex" [MeSH:National Library of Medicine - Medical Subject Headings , 2003, Principles of Neural Science , 3rd edition:ISBN 0-8385-8034-3] |
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Allelic Composition: Gli2tm2.1Alj/Gli2tm3.1(Gli1)Alj,Shhtm1Chg/Shhtm1Chg Genetic Background: either: (involves: 129) or (involves: 129 * Black Swiss)
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MP:0000849 | abnormal cerebellum morphology | "any malformation or absence of the part of the metencephalon that lies in the posterior cranial fossa dorsal to the pons and medulla that is concerned with the coordination of movement and learning of motor skills" [J:50311, Principles of Neural Science , 3rd edition:ISBN 0-8385-8034-3] |
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Allelic Composition: Ahrtm1Gonz/Ahrtm1Gonz Genetic Background: involves: 129S4/SvJae
Allelic Composition: Shhtm2Amc/Shhtm3Amc,Tg(Pax2-cre)1Amc/0 Genetic Background: involves: 129S1/Sv * 129X1/SvJ * Black Swiss
Allelic Composition: Shhtm1Chg/Shh+,Tg(Shh)#Dje/0 Genetic Background: involves: 129S1/Sv * 129X1/SvJ * Swiss Webster
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MP:0000851 | cerebellum hypoplasia | "reduced cell number in the cerebellum" [MGI:CLS, J:45302] |
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Allelic Composition: Shhtm1.1Rseg/Shhtm1.1Rseg Genetic Background: involves: 129S4/SvJae * C57BL/6
Allelic Composition: Shhtm1Amc/Shhtm1.1Rseg Genetic Background: involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6
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MP:0000852 | small cerebellum | "reduced size of cerebellum" [MGI:CLS, J:17203, J:67524] |
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Allelic Composition: Ahrtm1Gonz/Ahrtm1Gonz Genetic Background: involves: 129S4/SvJae
Allelic Composition: Shhtm2Amc/Shhtm3Amc,Tg(Pax2-cre)1Amc/0 Genetic Background: involves: 129S1/Sv * 129X1/SvJ * Black Swiss
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MP:0000854 | abnormal cerebellum development | "malformed or incomplete differentiation of the part of the metencephalon that lies dorsal to the pons and medulla behind the brain stem and controls balance for walking and standing, modulates the force and range of movement and is involved in the learning of motor skills " [MeSH:National Library of Medicine - Medical Subject Headings , 2003, Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8] |
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Allelic Composition: Ahrtm1Gonz/Ahrtm1Gonz Genetic Background: involves: 129S4/SvJae
Allelic Composition: Shhtm2Amc/Shhtm3Amc,Tg(Pax2-cre)1Amc/0 Genetic Background: involves: 129S1/Sv * 129X1/SvJ * Black Swiss
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MP:0000872 | abnormal external granule cell layer | "malformation of the transient layer of the cerebellar cortex which is composed of the dividing and migrating granule cells" [tc:Teresa Chu , Mouse Genome Informatics Curator] |
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Allelic Composition: Shhtm2Amc/Shhtm3Amc,Tg(Pax2-cre)1Amc/0 Genetic Background: involves: 129S1/Sv * 129X1/SvJ * Black Swiss
Allelic Composition: Shhtm1.1Rseg/Shhtm1.1Rseg Genetic Background: involves: 129S4/SvJae * C57BL/6
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MP:0000873 | thin external granule cell layer | "reduced thickness of the transient layer of the cerebellar cortex which is composed of dividing and migrating granule cells" [tc:Teresa Chu , Mouse Genome Informatics Curator, J:60896] |
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Allelic Composition: Ahrtm1Gonz/Ahrtm1Gonz Genetic Background: involves: 129S4/SvJae
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MP:0000875 | abnormal cerebellar Purkinje cell layer | "any malformation or absence of the cell layer that lies just underneath the molecular layer of the cerebellar cortex; it contains the neuronal cell bodies of the Purkinje cells that are arranged side by side in a single layer, and candelabrum interneurons are vertically oriented between the Purkinje cells" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8] |
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Allelic Composition: Ahrtm1Gonz/Ahrtm1Gonz Genetic Background: involves: 129S4/SvJae
Allelic Composition: Shhtm2Amc/Shhtm3Amc,Tg(Pax2-cre)1Amc/0 Genetic Background: involves: 129S1/Sv * 129X1/SvJ * Black Swiss
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MP:0000880 | decreased Purkinje cell number | "fewer than normal neuronal cells that are located in the interface of the molecular and granular layers of the cerebellar cortex" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, J:45302] |
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Allelic Composition: Ahrtm1Gonz/Ahrtm1Gonz Genetic Background: involves: 129S4/SvJae
Allelic Composition: Shhtm2Amc/Shhtm3Amc,Tg(Pax2-cre)1Amc/0 Genetic Background: involves: 129S1/Sv * 129X1/SvJ * Black Swiss
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MP:0000886 | abnormal cerebellar granule layer | "any malformation or absence of the innermost cortical layer of the cerebellum; contains densly packed small neurons, mostly granule cells with some Golgi cells are found at the outer border" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, Principles of Neural Science , 3rd edition:ISBN 0-8385-8034-3] |
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Allelic Composition: Shhtm2Amc/Shhtm3Amc,Tg(Pax2-cre)1Amc/0 Genetic Background: involves: 129S1/Sv * 129X1/SvJ * Black Swiss
Allelic Composition: Shhtm1Chg/Shh+,Tg(Shh)#Dje/0 Genetic Background: involves: 129S1/Sv * 129X1/SvJ * Swiss Webster
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MP:0000889 | abnormal cerebellar molecular layer | "any malformation or absence of the outermost layer of the cerebral cortex that contains the parallel fibers of the granule cells, interneurons such as stellate and basket cells, and the dendrites of the underlying Purkinje cells" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:38857] |
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Allelic Composition: Shhtm2Amc/Shhtm3Amc,Tg(Pax2-cre)1Amc/0 Genetic Background: involves: 129S1/Sv * 129X1/SvJ * Black Swiss
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MP:0000897 | abnormal midbrain | "malformation or malfunction associated with the middle of the three cerebral vesicles of the embryo; this region controls sensory and motor functions, including eye movement and coordination of auditory and visual reflexes" [J:23882, Principles of Neural Science , 3rd edition:ISBN 0-8385-8034-3] |
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Allelic Composition: Ndst1tm1.1Grob/Ndst1tm1.1Grob,Shhtm1Chg/Shh+ Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Allelic Composition: Wnt1tm1.1Mze/Wnt1tm1.1Mze,Gt(ROSA)26Sortm14(CAG-tdTomato)Hze/Gt(ROSA)26Sor+,Shhtm1(EGFP/cre)Cjt/Shh+ Genetic Background: involves: 129S6/SvEvTac * C57BL/6N
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MP:0000914 | exencephaly | "neurocranial defects resulting in exposure or extrusion of the brain" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:49840] |
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Allelic Composition: Shhtm1Chg/Shhtm1Chg,Tulp3hhkr/Tulp3hhkr Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C3H/HeH * C57BL/6
Allelic Composition: Ift122sopb/Ift122sopb,Shhtm1Chg/Shhtm1Chg Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C3HeB/FeJ * C57BL/6J
Allelic Composition: Shhtm1Chg/Shhtm1Chg,Tmem107schlei/Tmem107schlei Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C3HeB/FeJ * C57BL/6J
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MP:0000925 | abnormal floor plate morphology | "malformation or absence of a transient group of neuroepithelial cells located at the ventral midline of the neural tube that profoundly influences the development of the vertebrate central nervous system" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
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Allelic Composition: Gas1tm2Fan/Gas1tm2Fan,Shhtm1Chg/Shh+ Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6J
Allelic Composition: Shhtm1Chg/Shhtm1Chg,Tmem107schlei/Tmem107schlei Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C3HeB/FeJ * C57BL/6J
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MP:0000926 | absent floor plate | "missing ventral midline thinning of the developing neural tube" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:35802] |
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Allelic Composition: Fgfr2tm1.1Dsn/Fgfr2+ Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Allelic Composition: Gli2tm2.1Alj/Gli2tm2.1Alj,Shhtm1Chg/Shhtm1Chg Genetic Background: either: (involves: 129) or (involves: 129 * Black Swiss)
Allelic Composition: Disp1icb/Disp1tm2Amc,Shhtm1(EGFP/cre)Cjt/Shh+ Genetic Background: involves: 129/Sv * C57BL/6J * SWR
Allelic Composition: Disp1tm2.1Amc/Disp1tm2.1Amc,Shhtm1Amc/Shh+ Genetic Background: involves: 129/Sv * C57BL/6J * SWR
Allelic Composition: Gli2tm2.1Alj/Gli2tm3.1(Gli1)Alj,Shhtm1Chg/Shhtm1Chg Genetic Background: either: (involves: 129) or (involves: 129 * Black Swiss)
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MP:0000929 | open neural tube | "incomplete invagination and fusion of the neuroepithelial layer in early development" [MGI:CLS, J:53370, J:62571] |
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Allelic Composition: Ift122sopb/Ift122sopb,Shhtm1Chg/Shhtm1Chg Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C3HeB/FeJ * C57BL/6J
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MP:0000932 | absent notochord | "missing axial fibrocellular cord in embryos around which develops the vertebral primordia" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:12622] |
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Allelic Composition: Fkbp8tm1Tili/Fkbp8tm1Tili,Shhtm1Chg/Shhtm1Chg Genetic Background: involves: C57BL/6
Allelic Composition: Shhtm1Chg/Shhtm1Chg Genetic Background: involves: C57BL/6
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MP:0000934 | abnormal telencephalon development | "malformed or incomplete differentiation of the anterior division of the embryonic prosencephalon " [Stedman s Medical Dictionary:ISBN 0-683-40008-8, MGI:CLS, J:49840] |
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Allelic Composition: Cd19tm1(cre)Cgn/Cd19+,Gt(ROSA)26Sortm4(Ikbkb)Rsky/Gt(ROSA)26Sor+ Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Allelic Composition: Gli2tm2.1Alj/Gli2+,Shhtm1Chg/Shhtm1Chg Genetic Background: either: (involves: 129) or (involves: 129 * Black Swiss)
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MP:0000937 | abnormal motor neuron morphology | "malformation or absence of cells that innervate an effector (muscle or glandular) tissue; responsible for transmission of motor impulses" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, MGI:CLS, J:60159] |
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Allelic Composition: Fgfr2tm1.1Dsn/Fgfr2+ Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Allelic Composition: Shhtm1Chg/Shhtm1Chg Genetic Background: involves: C57BL/6
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MP:0000939 | reduced motor neuron number | "fewer than normal numbers of cells that innervate an effector (muscle or glandular) tissue" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, MGI:CLS, J:60159] |
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Allelic Composition: Fgfr2tm1.1Dsn/Fgfr2+ Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Allelic Composition: Gli2tm2.1Alj/Gli2tm2.1Alj,Shhtm1Chg/Shhtm1Chg Genetic Background: either: (involves: 129) or (involves: 129 * Black Swiss)
Allelic Composition: Shhtm1Ptch/Shhtm1Ptch Genetic Background: involves: 129P2/OlaHsd * FVB/N * various
Allelic Composition: Gli2tm2.1Alj/Gli2tm3.1(Gli1)Alj,Shhtm1Chg/Shhtm1Chg Genetic Background: either: (involves: 129) or (involves: 129 * Black Swiss)
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MP:0000955 | abnormal spinal cord morphology | "malformation or disorganization of the cylindrical tissue of the vertebral canal that extends from the medulla oblongata to the conus medullaris" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
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Allelic Composition: Gli2tm2.1Alj/Gli2+,Shhtm1Chg/Shhtm1Chg Genetic Background: either: (involves: 129) or (involves: 129 * Black Swiss)
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MP:0000956 | reduced spinal cord size | "smaller appearance of the spinal cord" [J:35802] |
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Allelic Composition: Fgfr2tm1.1Dsn/Fgfr2+ Genetic Background: involves: 129P2/OlaHsd * C57BL/6
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MP:0001046 | abnormal enteric neuron morphology | "malformed or absent neurons that innervate the esophagus, stomach, small and large bowel" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
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Allelic Composition: Shhtm1Amc/Shhtm1Amc Genetic Background: involves: 129/Sv * C57BL/6J * CBA/J
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MP:0001175 | abnormal lung morphology | "malformed organ of respiration" [J:35802] |
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Allelic Composition: Fgfr2tm1.1Dsn/Fgfr2+ Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Allelic Composition: Shhtm2Amc/Shhtm2Amc,Tg(SFTPC-rtTA)5Jaw/0,Tg(tetO-cre)1Jaw/0 Genetic Background: involves: FVB/N
Allelic Composition: Shhtm1Amc/Shhtm2Amc,Tg(SFTPC-rtTA)5Jaw/0,Tg(tetO-cre)1Jaw/0 Genetic Background: involves: FVB/N
Allelic Composition: Gt(ROSA)26Sortm1(tetO-Sox9)Msan/Gt(ROSA)26Sortm1(rtTA,EGFP)Nagy,Shhtm1(EGFP/cre)Cjt/Shh+ Genetic Background: involves: 129S1/Sv * 129X1/SvJ
Allelic Composition: Yy1tm2.1Yshi/Yy1tm2.1Yshi,Shhtm1(EGFP/cre)Cjt/Shh+ Genetic Background: involves: 129S4/SvJae * C57BL/6
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MP:0001176 | abnormal lung development | "malformation or arrest of differentiation of the organs of respiration" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:54931] |
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Allelic Composition: Irx4tm1Jse/Irx4+ Genetic Background: involves: 129X1/SvJ * Black Swiss
Allelic Composition: Ctnnb1tm2Kem/Ctnnb1tm2Kem,Shhtm1(EGFP/cre)Cjt/Shh+ Genetic Background: involves: 129S1/Sv * 129X1/SvJ
Allelic Composition: Dicer1tm1Bdh/Dicer1tm1Bdh,Shhtm1(EGFP/cre)Cjt/Shh+ Genetic Background: involves: 129
Allelic Composition: Ctnnb1tm1Mmt/Ctnnb1tm1Mmt,Shhtm1(EGFP/cre)Cjt/Shh+ Genetic Background: involves: 129X1/SvJ
Allelic Composition: Yy1tm2.1Yshi/Yy1tm2.1Yshi,Shhtm1(EGFP/cre)Cjt/Shh+ Genetic Background: involves: 129S4/SvJae * C57BL/6
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MP:0001178 | pulmonary hypoplasia | "reduced size of the respiratory organ due to incomplete development of all or part of the organ " [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator, Pathology , 2nd edition:ISBN 0-397-51047-0] |
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Allelic Composition: Ednratm1Ywa/Ednratm1Ywa Genetic Background: involves: 129S7/SvEvBrd
Allelic Composition: Shhtm2Amc/Shhtm2Amc,Tg(SFTPC-rtTA)5Jaw/0,Tg(tetO-cre)1Jaw/0 Genetic Background: involves: FVB/N
Allelic Composition: Shhtm1Amc/Shhtm2Amc,Tg(SFTPC-rtTA)5Jaw/0,Tg(tetO-cre)1Jaw/0 Genetic Background: involves: FVB/N
Allelic Composition: Shhtm1Amc/Shhtm1Amc Genetic Background: involves: 129/Sv * C57BL/6J * CBA/J
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MP:0001181 | absent lungs | "missing organs of respiration" [J:51966, J:50768] |
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Allelic Composition: Ctnnb1tm2Kem/Ctnnb1tm2Kem,Shhtm1(EGFP/cre)Cjt/Shh+ Genetic Background: involves: 129S1/Sv * 129X1/SvJ
Allelic Composition: Ctnnb1tm1Mmt/Ctnnb1tm1Mmt,Shhtm1(EGFP/cre)Cjt/Shh+ Genetic Background: involves: 129X1/SvJ
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MP:0001218 | thin epidermis | "reduced thickness of the superficial epithelial portion of the skin" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:61790] |
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Allelic Composition: Slc17a8tm1Edw/Slc17a8+ Genetic Background: involves: 129P2/OlaHsd * C57BL/6
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MP:0001219 | thickened epidermis | "increase in the width of the epidermal cell layer in the skin" [J:65146] |
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Allelic Composition: Shhtm1Amc/Shhtm1Amc Genetic Background: involves: 129/Sv * C57BL/6J * CBA/J
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MP:0001222 | epidermal hyperplasia | "increase in size of the epidermis due to increase in epidermal cell number" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:65146] |
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Allelic Composition: Shhtm1Amc/Shhtm1Amc Genetic Background: involves: 129/Sv * C57BL/6J * CBA/J
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MP:0001243 | abnormal dermal layer morphology | "malformed or atypical condition of the dermal layer of the skin" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:56777] |
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Allelic Composition: Irx4tm1Jse/Irx4+ Genetic Background: involves: 129X1/SvJ * Black Swiss
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MP:0001262 | decreased body weight | "lower than normal average weight " [J:61295] |
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Allelic Composition: Efnb3tm1.1Henk/Efnb3tm1.1Henk Genetic Background: involves: 129S1/Sv * 129X1/SvJ * CD-1
Allelic Composition: Shhtm1Amc/Shhtm1.1Rseg Genetic Background: involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6
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MP:0001265 | reduced body size | "smaller than average body weight, height and/or length of an organism compared to controls" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, J:23170] |
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Allelic Composition: Stat4tm1Gru/Stat4tm1Gru Genetic Background: C.129S2-Stat4tm1Gru
Allelic Composition: Pofut1tm2Pst/Pofut1tm1Pst,Shhtm2(cre/ERT2)Cjt/Shh+ Genetic Background: involves: 129/Sv * 129S6/SvEvTac * C57BL/6J * SJL
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MP:0001284 | absent vibrissae | "missing whiskers" [J:18378] |
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Allelic Composition: Shhtm1Amc/Shhtm2Amc,Tg(KRT14-cre)1Amc/0 Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA
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MP:0001286 | abnormal eye development | "malformation or arrest of differentiation of the visual organ" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, MGI:cls, J:49840] |
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Allelic Composition: Chd7Whi/Chd7+ Genetic Background: C3HeB/FeJ-Chd7Whi
Allelic Composition: Shhtm1Amc/Shhtm2Amc,Tg(Thy1-cre)703Vaw/? Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C3H * C57BL/6
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MP:0001293 | anophthalmia | "congenital absence of all tissues of the eyes" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, MGI:CML, J:71979] |
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Allelic Composition: ShhDsh/ShhDsh Genetic Background: involves: 101 * C3H * C57BL * SEC
Allelic Composition: Shhtm1Chg/Shh+,Sulf1Gt(XM190)Byg/Sulf1Gt(XM190)Byg,Sulf2Gt(PST111)Byg/Sulf2Gt(PST111)Byg Genetic Background: involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/10
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MP:0001297 | microphthalmia | "reduced average size of the eyes" [J:18048] |
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Allelic Composition: Fkbp8tm1Tili/Fkbp8tm1Tili,Shhtm1Chg/Shhtm1Chg Genetic Background: involves: C57BL/6
Allelic Composition: Ndst1tm1.1Grob/Ndst1+,Shhtm1Chg/Shh+ Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Allelic Composition: Shhtm1Amc/Shhtm2Amc,Tg(Thy1-cre)703Vaw/? Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C3H * C57BL/6
Allelic Composition: Shhtm1Chg/Shh+,Sulf1Gt(XM190)Byg/Sulf1Gt(XM190)Byg,Sulf2Gt(PST111)Byg/Sulf2Gt(PST111)Byg Genetic Background: involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/10
Allelic Composition: Shhtm1.1Rseg/Shhtm1.1Rseg Genetic Background: involves: 129S4/SvJae * C57BL/6
Allelic Composition: Shhtm1Amc/Shhtm1.1Rseg Genetic Background: involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6
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MP:0001302 | eyelids open at birth | "widely open eyes instead of closed at perinatal stage" [J:51966] |
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Allelic Composition: Shhtm1Amc/Shhtm2Amc,Tg(KRT14-cre)1Amc/0 Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA
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MP:0001325 | abnormal retina morphology | "structural or developmental anomaly of the thin layer of neural tissue lining the back of the eyeball which contains visual receptors " [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator] |
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Allelic Composition: Shhtm1Amc/Shhtm2Amc,Tg(Thy1-cre)703Vaw/? Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C3H * C57BL/6
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MP:0001330 | abnormal optic nerve morphology | "malformation, misprojection or atrophy in the second cranial nerve which is responsible for conveying visual information from the retina to the brain" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
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Allelic Composition: Shhtm1Amc/Shhtm2Amc,Tg(Thy1-cre)703Vaw/? Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C3H * C57BL/6
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MP:0001340 | abnormal eyelid morphology | "malformation of the skin folds covering the front of the eyeball" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
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Allelic Composition: Shhtm1Amc/Shhtm2Amc,Tg(Thy1-cre)703Vaw/? Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C3H * C57BL/6
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MP:0001393 | ataxia | "inability to coordinate voluntary muscular movements" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:67231] |
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Allelic Composition: Ahrtm1Gonz/Ahrtm1Gonz Genetic Background: involves: 129S4/SvJae
Allelic Composition: Shhtm2Amc/Shhtm3Amc,Tg(Pax2-cre)1Amc/0 Genetic Background: involves: 129S1/Sv * 129X1/SvJ * Black Swiss
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MP:0001399 | hyperactivity | "general restlessness or excessive movement; more frequent movement from one place to another" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:60409, J:57125] |
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Allelic Composition: Shhtm1Ahk/Shhtm1Ahk,Slc6a3tm1(cre)Xz/Slc6a3+ Genetic Background: involves: 129S1/Sv * C57BL/6
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MP:0001402 | hypoactivity | "reduced movement from one place to another" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, csmith:Cynthia L. Smith , Mouse Genome Informatics Curator, J:64289] |
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Allelic Composition: Shhtm1Ahk/Shhtm1Ahk,Slc6a3tm1(cre)Xz/Slc6a3+ Genetic Background: involves: 129S1/Sv * C57BL/6
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MP:0001406 | abnormal gait | "unusual or distinctive way of walking" [J:65038] |
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Allelic Composition: Shhtm1Ahk/Shhtm1Ahk,Slc6a3tm1(cre)Xz/Slc6a3+ Genetic Background: involves: 129S1/Sv * C57BL/6
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MP:0001622 | abnormal vasculogenesis | "aberrant process of the initial establishment of the vascular network " [J:67296, csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
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Allelic Composition: Lamp1tm1Psa/Lamp1tm1Psa,Lamp2tm1Psa/Y Genetic Background: involves: 129P2/OlaHsd * C57BL/6
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MP:0001672 | abnormal embryogenesis/ development | "anomaly in the establishment of the characteristic configuration of the embryonic body" [Stedman s Medical Dictionary:ISBN 0-683-40008-8] |
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Allelic Composition: Shhtm3(cre)Chg/Shhtm3(cre)Chg Genetic Background: Not Specified
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MP:0001691 | abnormal somite shape | "atypical characteristic surface configuration of a segmental mass along the notochord of the developing embryo" [J:37888] |
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Allelic Composition: Fkbp8tm1Tili/Fkbp8tm1Tili,Shhtm1Chg/Shhtm1Chg Genetic Background: involves: C57BL/6
Allelic Composition: Shhtm1Chg/Shhtm1Chg Genetic Background: involves: C57BL/6
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MP:0001697 | abnormal embryo size | "anomalous proportions of embryo compared to littermates" [cwg:Carroll W. Goldsmith, Mouse Genome Informatics Curator] |
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Allelic Composition: ShhDsh/ShhDsh Genetic Background: involves: 101 * C3H * C57BL * SEC
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MP:0001698 | reduced embryo size | "smaller proportions of embryo compared to littermates" [J:61790] |
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Allelic Composition: Shhtm1Ptch/Shhtm1Ptch Genetic Background: involves: 129P2/OlaHsd * FVB/N * various
Allelic Composition: ShhDsh/ShhDsh Genetic Background: B10Rl.Cg-ShhDsh
Allelic Composition: Gas1tm2Fan/Gas1tm2Fan,Shhtm1Chg/Shhtm1Chg Genetic Background: involves: 129/Sv * 129S1/Sv * 129X1/SvJ * C57BL/6J
Allelic Composition: Gli2tm2.1Alj/Gli2+,Shhtm1Chg/Shhtm1Chg Genetic Background: either: (involves: 129) or (involves: 129 * Black Swiss)
Allelic Composition: Shhtm1Chg/Shhtm1Chg,Zic2Ku/Zic2Ku Genetic Background: involves: 129S1/Sv * 129X1/SvJ * BALB/cAnNCrl * C3H/HeH
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MP:0001700 | abnormal embryo turning | "atypical axial rotation of the germ layers of the embryo during the primitive streak/early somite stage (Mus:E8.5-E9.5) such that the curvature of the entire trunk region is reversed and the neural ectoderm moves to the convex region and the midgut region becomes located in the concave region" [The Atlas of Mouse Development:ISBN 0-12-402035-6, csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
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Allelic Composition: Gas1tm2Fan/Gas1tm2Fan,Shhtm1Chg/Shhtm1Chg Genetic Background: involves: 129/Sv * 129S1/Sv * 129X1/SvJ * C57BL/6J
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MP:0001704 | abnormal dorsal-ventral axis patterning | "anomaly in the development or formation of the axis that runs from the front to the back surface of the body" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
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Allelic Composition: Fgfr2tm1.1Dsn/Fgfr2+ Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Allelic Composition: Fkbp8tm1Tili/Fkbp8tm1Tili,Shhtm1Chg/Shhtm1Chg Genetic Background: involves: C57BL/6
Allelic Composition: Shhtm1Chg/Shhtm1Chg Genetic Background: involves: C57BL/6
Allelic Composition: ShhDsh/Shhtm1Chg Genetic Background: involves: 101 * 129S1/Sv * 129X1/SvJ * C3H * C57BL/10Rl
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MP:0001718 | abnormal yolk sac | "malformed extraembryonic tissue which contributes to hematopoietic circulation" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, MGI:cls, J:12623] |
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Allelic Composition: Tyrc-32DSD/Tyrc Genetic Background: involves: 101/Rl * C3H/Rl
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MP:0001719 | absent vitelline blood vessels | "missing vasculature of the yolk sac" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:62571, J:12623] |
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Allelic Composition: Tyrc-32DSD/Tyrc Genetic Background: involves: 101/Rl * C3H/Rl
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MP:0001730 | embryonic growth arrest | "the cessation of development beyond a particular stage" [J:17509] |
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Allelic Composition: Trp53tm1Tyj/Trp53tm1Tyj Genetic Background: involves: 129S2/SvPas
Allelic Composition: Gas1tm2Fan/Gas1tm2Fan,Shhtm1Chg/Shhtm1Chg Genetic Background: involves: 129/Sv * 129S1/Sv * 129X1/SvJ * C57BL/6J
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MP:0001732 | postnatal growth retardation | "slow or limited development after birth " [Stedman s Medical Dictionary:ISBN 0-683-40008-8] |
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Allelic Composition: Shhtm2Amc/Shhtm2Amc,Tg(Nes-cre)1Kln/0 Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL
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MP:0001748 | increased circulating adrenocorticotropin level | "elevated concentration in the blood of the pituitary hormone that stimulates the secretion of adrenal cortical steroids and induces growth of the adrenal cortex
" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, MGI:cls, J:54931] |
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Allelic Composition: Edardl-J/Edardl-J Genetic Background: involves: C3HeB/FeJ
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MP:0001785 | edema | "an accumulation of an excessive amount of watery fluid in cells or intercellular tissues" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:54065] |
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Allelic Composition: Shhtm1Chg/Shhtm1Chg,Tulp3hhkr/Tulp3hhkr Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C3H/HeH * C57BL/6
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MP:0001861 | lung inflammation | "local accumulation of fluid, plasma proteins, and leukocytes in the lung" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator, Immunobiology , The Immune System in Health and Disease:ISBN 0-8153-1691-7] |
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Allelic Composition: Pofut1tm2Pst/Pofut1tm1Pst,Shhtm2(cre/ERT2)Cjt/Shh+ Genetic Background: involves: 129/Sv * 129S6/SvEvTac * C57BL/6J * SJL
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MP:0001906 | increased dopamine level | "greater than the normal concentration of this catecholamine neurotransmitter, dervied from tyrosine and the precursor to norepinephrine and epinephrine" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator, MeSH:National Library of Medicine - Medical Subject Headings , 2003] |
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Allelic Composition: Shhtm1Ahk/Shhtm1Ahk,Slc6a3tm1(cre)Xz/Slc6a3+ Genetic Background: involves: 129S1/Sv * C57BL/6
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MP:0001919 | abnormal reproductive system physiology | "anomaly in the function of the organs associated with producing offspring " [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
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Allelic Composition: Il1r1tm1.1Rbl/Il1r1tm1.1Rbl Genetic Background: B6.129(Cg)-Il1r1tm1.1Rbl
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MP:0001953 | respiratory failure | "cessation of or failure to commence breathing" [MGI:cls, J:60159] |
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Allelic Composition: Yy1tm2.1Yshi/Yy1tm2.1Yshi,Shhtm1(EGFP/cre)Cjt/Shh+ Genetic Background: involves: 129S4/SvJae * C57BL/6
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MP:0001954 | respiratory distress | "physical difficulty or inability to breathe" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:54931] |
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Allelic Composition: Tmem107schlei/Tmem107tm1Lex Genetic Background: involves: 129S5/SvEvBrd * C3HeB/FeJ * C57BL/6J * C57BL/6N
Allelic Composition: Sox9tm1Gsr/Sox9tm1Gsr,Shhtm1(EGFP/cre)Cjt/Shh+ Genetic Background: involves: 129P2/OlaHsd
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MP:0002058 | neonatal lethality | "death of animal within one day after birth" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
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Allelic Composition: Disp1tm2Amc/Disp1tm2Amc Genetic Background: involves: 129/Sv * C57BL/6J * SWR
Allelic Composition: Disp1icb/Disp1tm2Amc,Shhtm1(EGFP/cre)Cjt/Shh+ Genetic Background: involves: 129/Sv * C57BL/6J * SWR
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MP:0002060 | abnormal skin morphology | "malformation or atypical structure of the membranous protective covering of the body" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, J:56777] |
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Allelic Composition: Slc17a8tm1Edw/Slc17a8+ Genetic Background: involves: 129P2/OlaHsd * C57BL/6
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MP:0002064 | seizures | "sudden and often acute manifestation of epileptic attack, sometimes convulsive" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
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Allelic Composition: Stat4tm1Gru/Stat4tm1Gru Genetic Background: C.129S2-Stat4tm1Gru
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MP:0002066 | abnormal motor capabilities/coordination/movement | "altered ability to coordinate voluntary movement or repetitive, compulsive movements" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
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Allelic Composition: Ahrtm1Gonz/Ahrtm1Gonz Genetic Background: involves: 129S4/SvJae
Allelic Composition: Shhtm2Amc/Shhtm3Amc,Tg(Pax2-cre)1Amc/0 Genetic Background: involves: 129S1/Sv * 129X1/SvJ * Black Swiss
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MP:0002080 | prenatal lethality | "death anytime between fertilization and E18.5" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
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Allelic Composition: Ndst1tm1.1Grob/Ndst1+,Shhtm1Chg/Shh+ Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
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MP:0002081 | perinatal lethality | "death anytime between E18.5 and postnatal day 1 " [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
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Allelic Composition: Cd19tm1(cre)Cgn/Cd19+,Gt(ROSA)26Sortm4(Ikbkb)Rsky/Gt(ROSA)26Sor+ Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Allelic Composition: Shhtm3(cre)Chg/Shhtm3(cre)Chg Genetic Background: Not Specified
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MP:0002083 | premature death | "death after 3 weeks of age, but before normal life span" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
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Allelic Composition: Ccd/Ccd+,ShhDsh/Shh+ Genetic Background: involves: 101 * C3H * C57BL * C57BL/10Rl * SEC
Allelic Composition: Shhtm2Amc/Shhtm3Amc,Tg(Pax2-cre)1Amc/0 Genetic Background: involves: 129S1/Sv * 129X1/SvJ * Black Swiss
Allelic Composition: Pofut1tm2Pst/Pofut1tm1Pst,Shhtm2(cre/ERT2)Cjt/Shh+ Genetic Background: involves: 129/Sv * 129S6/SvEvTac * C57BL/6J * SJL
Allelic Composition: Shhtm1Ahk/Shhtm1Ahk,Slc6a3tm1(cre)Xz/Slc6a3+ Genetic Background: involves: 129S1/Sv * C57BL/6
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MP:0002092 | abnormal eye morphology | "abnormal development of the eye tissues resulting in morphological abnormality or abnormal structure of the visual system" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
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Allelic Composition: Shhtm3(cre)Chg/Shhtm3(cre)Chg Genetic Background: Not Specified
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MP:0002102 | abnormal ear morphology | "structural or developmental anomaly of any of the structures involved in the ear or vestibular system" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
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Allelic Composition: ShhDsh/Shh+ Genetic Background: B10Rl.Cg-ShhDsh
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MP:0002109 | abnormal limb morphology | "abnormal development of limbs resulting in morphological abnormality" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
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Allelic Composition: Ppargtm1.2Mtz/Ppargtm1.2Mtz,Tg(Fabp4-cre/ERT2)1Ipc/0 Genetic Background: involves: C57BL/6
Allelic Composition: Shhtm1Chg/Shhtm1Chg Genetic Background: involves: C57BL/6
Allelic Composition: ShhDsh/Shhtm1Chg Genetic Background: involves: 101 * 129S1/Sv * 129X1/SvJ * C3H * C57BL/10Rl
Allelic Composition: Gli3tm2Blnw/Gli3+,Shhtm1Chg/Shhtm1Chg Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N
Allelic Composition: ShhDz/ShhDz Genetic Background: C57BL/6J-ShhDz
Allelic Composition: Rr29tm1.1Bobh/Rr29+,Shhtm1Chg/Shh+ Genetic Background: involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ
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MP:0002110 | abnormal digit morphology | "abnormal development of the digits resulting in structural abnormality" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
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Allelic Composition: Cd19tm1(cre)Cgn/Cd19+,Gt(ROSA)26Sortm4(Ikbkb)Rsky/Gt(ROSA)26Sor+ Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Allelic Composition: Disp1tm1Pab/Disp1tm1Pab,Shhtm2Chg/Shh+,Edil3Tg(Sox2-cre)1Amc/Edil3+ Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA
Allelic Composition: Gli3tm2Blnw/Gli3+,Shhtm1Chg/Shhtm1Chg Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N
Allelic Composition: Gt(ROSA)26Sortm5(Etv4/en,-GFP)Amc/Gt(ROSA)26Sor+,Shhtm1Amc/Shhtm2Amc,Tg(Prrx1-cre)1Cjt/0 Genetic Background: involves: 129 * C57BL/6 * CBA * SJL/J * Swiss Webster
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MP:0002114 | abnormal axial skeleton morphology | "abnormal development of vertebral, spinal or sternal bones resulting in morphological abnormality" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
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Allelic Composition: Fgfr2tm1.1Dsn/Fgfr2+ Genetic Background: involves: 129P2/OlaHsd * C57BL/6
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MP:0002115 | abnormal skeleton extremities morphology | "abnormal development of limb, foot or tail bones resulting in morphological abnormality" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
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Allelic Composition: Lamp1tm1Psa/Lamp1tm1Psa,Lamp2tm1Psa/Y Genetic Background: involves: 129P2/OlaHsd * C57BL/6
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MP:0002116 | abnormal craniofacial bone morphology | "abnormal development of cranial or facial bones resulting in morphological abnormality" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
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Allelic Composition: Fgfr2tm1.1Dsn/Fgfr2+ Genetic Background: involves: 129P2/OlaHsd * C57BL/6
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MP:0002127 | abnormal cardiovascular system morphology | "abnormal development of the heart or vascular tissue resulting in morphological abnormality" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
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Allelic Composition: Shhtm3(cre)Chg/Shhtm3(cre)Chg Genetic Background: Not Specified
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MP:0002132 | abnormal respiratory system morphology | "anomalous structure of pulmonary tissues " [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
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Allelic Composition: Shhtm3(cre)Chg/Shhtm3(cre)Chg Genetic Background: Not Specified
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MP:0002135 | abnormal kidney morphology | "abnormal development of the kidney resulting in structural abnormality" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
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Allelic Composition: Fgfr2tm1.1Dsn/Fgfr2+ Genetic Background: involves: 129P2/OlaHsd * C57BL/6
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MP:0002151 | abnormal neural tube morphology/development | "anomalous structure of or development of the embryonic neural tube resulting in structural anomaly" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
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Allelic Composition: Fgfr2tm1.1Dsn/Fgfr2+ Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Allelic Composition: Fkbp8tm1Tili/Fkbp8tm1Tili,Shhtm1Chg/Shhtm1Chg Genetic Background: involves: C57BL/6
Allelic Composition: Shhtm1Chg/Shhtm1Chg Genetic Background: involves: C57BL/6
Allelic Composition: Shhtm1(EGFP/cre)Cjt/Shhtm2Amc Genetic Background: involves: 129/Sv * C57BL/6J * SWR
Allelic Composition: Shhtm1Chg/Shhtm1Chg,Tulp3hhkr/Tulp3hhkr Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C3H/HeH * C57BL/6
Allelic Composition: Ift122sopb/Ift122sopb,Shhtm1Chg/Shhtm1Chg Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C3HeB/FeJ * C57BL/6J
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MP:0002169 | no phenotype detected | "normal, viable and fertile appearance and behavior; indistinguishable from controls" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
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Allelic Composition: Shhtm1Amc/Shhtm2Amc,Tg(KRT14-cre)1Amc/0 Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA
Allelic Composition: Ptch1tm1Mps/Ptch1+,Shhtm6Amc/Shhtm6Amc Genetic Background: involves: 129S1/Sv * 129X1/SvJ
Allelic Composition: Shhtm1(cre/ERT2)Tshim/Shhtm1(cre/ERT2)Tshim Genetic Background: Not Specified
Allelic Composition: Shhtm1Ahk/Shhtm1Ahk Genetic Background: B6.Cg-Shhtm1Ahk
Allelic Composition: Robo1tm1Matl/Robo1tm1Matl,Robo2tm1Rilm/Robo2tm1Rilm,Shhtm1(EGFP/cre)Cjt/Shh+ Genetic Background: involves: 129
Allelic Composition: Shh+/Shhtm1Chg,Zic2Ku/Zic2+ Genetic Background: involves: 129S1/Sv * 129X1/SvJ * BALB/cAnNCrl * C3H/HeH
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MP:0002175 | low brain weight | "lower than average weight of the brain" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
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Allelic Composition: Shhtm1.1Rseg/Shhtm1.1Rseg Genetic Background: involves: 129S4/SvJae * C57BL/6
Allelic Composition: Shhtm1Amc/Shhtm1.1Rseg Genetic Background: involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6
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MP:0002177 | abnormal outer ear morphology | "malformation or malfunction of any components of the auricles or external acoustic meatus" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
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Allelic Composition: Shhtm1Chg/Shh+,Vps25m1Lis/Vps25m1Lis Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C3H * C57BL/6J
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MP:0002182 | abnormal astrocyte morphology | "anomalous structure, number or compostion of one of the large neuroglia cells of nervous tissue" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
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Allelic Composition: Shhtm2Amc/Shhtm3Amc,Tg(Pax2-cre)1Amc/0 Genetic Background: involves: 129S1/Sv * 129X1/SvJ * Black Swiss
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MP:0002184 | abnormal innervation | "the malformation, misprojection or malfunction of the connection of nerve fibers with a target" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
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Allelic Composition: Gas1tm2Fan/Gas1tm2Fan,Shhtm1Chg/Shh+ Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6J
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MP:0002191 | abnormal artery morphology | "malformation of the blood vessels that carry blood away from the heart" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
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Allelic Composition: Nrp2tm1.2Mom/Nrp2+ Genetic Background: involves: 129P2/OlaHsd * C57BL/6 * FVB/NJ
Allelic Composition: Shhtm1Chg/Shhtm2Chg,Tg(Mef2c-cre)2Blk/0 Genetic Background: involves: 129S1/Sv * 129S7/SvEvBrd * 129X1/SvJ
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MP:0002196 | acallosal | "absence of the commissural plate interconnecting the cortical hemispheres of the brain" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
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Allelic Composition: Six3tm3.1Gco/Six3+,Shhtm1Chg/Shh+ Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
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MP:0002233 | abnormal nose morphology | "any structural anomaly of the organ that is specialized for smell and is part of the respiratory system " [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator, MeSH:National Library of Medicine - Medical Subject Headings , 2003] |
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Allelic Composition: Gas1tm2Fan/Gas1tm2Fan,Shhtm1Chg/Shh+ Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6J
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MP:0002234 | abnormal pharynx morphology | "structural anomaly in the passage between the mouth and the posterior nares and the larynx and esophagus" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator] |
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Allelic Composition: Ednratm1Ywa/Ednratm1Ywa Genetic Background: involves: 129S7/SvEvBrd
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MP:0002257 | abnormal arytenoid cartilage morphology | "any structural anomaly of the paired triangular cartilages located postlaterally at the level of the thyroid cartilage " [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator, Pathology , 2nd edition:ISBN 0-397-51047-0] |
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Allelic Composition: Ncr1m1J/Ncr1m1J,Pepcb/Pepcb,Ptprca/Ptprca Genetic Background: B6.SJL-Ptprca Pepcb/BoyJ
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MP:0002264 | abnormal bronchus morphology | "any structural anomaly of of the upper conducting airways of the lung; these airways arise from the terminus of the trachea " [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator, Pathology , 2nd edition:ISBN 0-397-51047-0, MeSH:National Library of Medicine - Medical Subject Headings , 2003] |
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Allelic Composition: Ednratm1Ywa/Ednratm1Ywa Genetic Background: involves: 129S7/SvEvBrd
Allelic Composition: Shhtm2Amc/Shhtm2Amc,Tg(SFTPC-rtTA)5Jaw/0,Tg(tetO-cre)1Jaw/0 Genetic Background: involves: FVB/N
Allelic Composition: Shhtm1Amc/Shhtm2Amc,Tg(SFTPC-rtTA)5Jaw/0,Tg(tetO-cre)1Jaw/0 Genetic Background: involves: FVB/N
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MP:0002282 | abnormal trachea morphology | "structral anomaly of the tube descending from the larynx and branching into the right and left main bronchi" [MeSH:National Library of Medicine - Medical Subject Headings , 2003, cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator] |
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Allelic Composition: Shhtm2Amc/Shhtm2Amc,Tg(SFTPC-rtTA)5Jaw/0,Tg(tetO-cre)1Jaw/0 Genetic Background: involves: FVB/N
Allelic Composition: Shhtm1Amc/Shhtm2Amc,Tg(SFTPC-rtTA)5Jaw/0,Tg(tetO-cre)1Jaw/0 Genetic Background: involves: FVB/N
Allelic Composition: Yy1tm2.1Yshi/Yy1tm2.1Yshi,Shhtm1(EGFP/cre)Cjt/Shh+ Genetic Background: involves: 129S4/SvJae * C57BL/6
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MP:0002284 | abnormal tracheal smooth muscle morphology | "structural anomaly of the smooth muscle lining the trachea" [Pathology:ISBN 0-397-51047-0, cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator] |
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Allelic Composition: Shhtm1Amc/Shhtm1Amc Genetic Background: involves: 129/Sv * C57BL/6J * CBA/J
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MP:0002285 | abnormal tracheal ciliated epithelium morphology | "structural anomaly of the epithelial lining of the trachea which contains numerous ciliated cells" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator, Pathology:ISBN 0-397-51047-0] |
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Allelic Composition: Yy1tm2.1Yshi/Yy1tm2.1Yshi,Shhtm1(EGFP/cre)Cjt/Shh+ Genetic Background: involves: 129S4/SvJae * C57BL/6
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MP:0002543 | brachyphalangia | "abnormally short phalanges" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8] |
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Allelic Composition: Irs2tm1Mfw/Irs2tm1Mfw Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6J
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MP:0002544 | brachydactyly | "abnormally short digits" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8] |
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Allelic Composition: Col4a3tm1Dec/Col4a3tm1Dec,Itga1tm1Gdnr/Itga1tm1Gdnr Genetic Background: involves: 129S4/SvJae * 129X1/SvJ * BALB/c
Allelic Composition: ShhDsh/Shh+ Genetic Background: B10Rl.Cg-ShhDsh
Allelic Composition: ShhDsh/ShhDsh Genetic Background: involves: 101 * C3H * C57BL * SEC
Allelic Composition: Ccd/Ccd+,ShhDsh/Shh+ Genetic Background: involves: 101 * C3H * C57BL * C57BL/10Rl * SEC
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MP:0002576 | abnormal enamel morphology | "malformation of the hard outer coating of the exposed portion of the tooth" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, J:71126, csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
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Allelic Composition: Shhtm1Amc/Shhtm2Amc,Tg(KRT14-cre)1Amc/0 Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA
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MP:0002633 | persistent truncus arteriosis | "complete failure of the common arterial trunk opening out of both ventricles to divide into the aorta and pulmonary artery during development" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, pvb:Pierre Vanden Borre , Mouse Genome Informatics Curator] |
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Allelic Composition: Shhtm1Chg/Shhtm2Amc,Nkx2-5tm1(cre)Rjs/Nkx2-5+ Genetic Background: involves: 129S1/Sv * 129S7/SvEvBrd * 129X1/SvJ
Allelic Composition: Shhtm1Chg/Shhtm2Chg,Tg(Mef2c-cre)2Blk/0 Genetic Background: involves: 129S1/Sv * 129S7/SvEvBrd * 129X1/SvJ
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MP:0002650 | abnormal ameloblast morphology | "malformation of the epithelial cells of the inner layer of the enamel organ of the developing tooth" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, il:Ira Lu , Mouse Genome Informatics Curator] |
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Allelic Composition: Shhtm1Amc/Shhtm2Amc,Tg(KRT14-cre)1Amc/0 Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA
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MP:0002665 | decreased circulating corticosterone level | "less than the normal blood concentration of this adrenocortical steroid; induces glycogen deposition and regulates sodium conservation and potassium secretion" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8] |
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Allelic Composition: Edardl-J/Edardl-J Genetic Background: involves: C3HeB/FeJ
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MP:0002691 | small stomach | "reduced size of the stomach" [J:77398, dlb:Donna Burkart , Mouse Genome Informatics Curator] |
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Allelic Composition: Ednratm1Ywa/Ednratm1Ywa Genetic Background: involves: 129S7/SvEvBrd
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MP:0002726 | abnormal pulmonary vein morphology | "structrual anomaly of the veins that return oxygenated blood from the lungs to the left atrium of the heart" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator] |
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Allelic Composition: Ctnnb1tm1Mmt/Ctnnb1tm1Mmt,Shhtm1(EGFP/cre)Cjt/Shh+ Genetic Background: involves: 129X1/SvJ
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MP:0002728 | absent tibia | "missing the medial and larger of the two bones of the lower leg" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, cml:Cathleen M. Lutz , Mouse Genome Informatics Curator] |
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Allelic Composition: Fgfr2tm1.1Dsn/Fgfr2+ Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Allelic Composition: Gli3tm2Blnw/Gli3+,Shhtm1Chg/Shhtm1Chg Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N
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MP:0002741 | small olfactory bulb | "reduced size of the forebrain region that coordinates neuronal signaling involved in the perception of smell; it receives input from the sensory neurons and outputs to the olfactory cortex" [J:79871] |
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Allelic Composition: Shhtm1.1Rseg/Shhtm1.1Rseg Genetic Background: involves: 129S4/SvJae * C57BL/6
Allelic Composition: Shhtm1Amc/Shhtm1.1Rseg Genetic Background: involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6
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MP:0002764 | short tibia | " reduced length of the medial and larger bone of the lower leg" [J:12736, pvb:Pierre Vanden Borre , Mouse Genome Informatics Curator] |
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Allelic Composition: Gli3tm2Blnw/Gli3+,Shhtm1Chg/Shhtm1Chg Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N
Allelic Composition: ShhDz/ShhDz Genetic Background: C57BL/6J-ShhDz
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MP:0002765 | short fibula | "reduced length of the lateral and smaller of bone of the lower leg" [pvb:Pierre Vanden Borre , Mouse Genome Informatics Curator, J:12736] |
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Allelic Composition: ShhDz/ShhDz Genetic Background: C57BL/6J-ShhDz
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MP:0002768 | small adrenal glands | "reduced size of endocrine glands located above the kidneys responsible for hormone and epinephrine secretion" [J:78062] |
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Allelic Composition: Edardl-J/Edardl-J Genetic Background: involves: C3HeB/FeJ
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MP:0002818 | abnormal dentin morphology | "defects in the hard portion of the tooth surrounding the pulp, covered by enamel on the crown and cementum on the root" [MeSH:National Library of Medicine - Medical Subject Headings , 2003] |
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Allelic Composition: Shhtm1Amc/Shhtm2Amc,Tg(KRT14-cre)1Amc/0 Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA
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MP:0002858 | abnormal posterior semicircular canal | "anomaly of the posterior segment of the long bony tube of the labyrinth that is involved in the sense of balance" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8] |
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Allelic Composition: Mdm2tm1Bay/Mdm2tm1Bay,Trp53tm1Snj/Trp53tm1Snj Genetic Background: involves: C57BL/6
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MP:0002898 | absent cartilage | "absence of the nonvascular, resilient, flexible connective tissue found primarily in joints, walls of the thorax, and tubular structures, but which also comprises most of the skeleton in early fetal life " [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8] |
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Allelic Composition: Fgfr2tm1.1Dsn/Fgfr2+ Genetic Background: involves: 129P2/OlaHsd * C57BL/6
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MP:0002908 | delayed wound healing | "longer time requirement for the ability to self-repair and close wounds than normal" [J:63037] |
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Allelic Composition: Brca2tm1Brn/Brca2tm1Brn,Trp53bp1tm1Jc/Trp53bp1tm1Jc,Cd19tm1(cre)Cgn/Cd19+ Genetic Background: involves: 129P2/OlaHsd
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MP:0002909 | abnormal adrenal gland physiology | "altered ability of the surparenal gland to produce and secrete hormones " [hdene:Howard Dene , Mouse Genome Informatics Curator] |
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Allelic Composition: Edardl-J/Edardl-J Genetic Background: involves: C3HeB/FeJ
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MP:0002932 | abnormal joint | "defect in the articulation point of two or more bones" [RGD:Rat Genome Database submission, MeSH:National Library of Medicine - Medical Subject Headings , 2003] |
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Allelic Composition: ShhDsh/Shh+ Genetic Background: B10Rl.Cg-ShhDsh
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MP:0002948 | abnormal neuronal specification | "defects in the developmental patterning of neurons resulting in ectopic placement, decreased numbers or absence of mature neurons" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator, J:87948] |
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Allelic Composition: Disp1icb/Disp1tm1Amc,Shhtm1Amc/Shh+ Genetic Background: involves: 129X1/SvJ * C57BL/6J
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MP:0002950 | abnormal neural crest cell migration | "defect in the dispersion of the transient and migratory group of cells that emerge from the dorsal region of the neural tube and migrate to many peripheral locations to form various tissues of the adult" [Principles of Neural Science , 3rd edition:ISBN 0-8385-8034-3] |
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Allelic Composition: Shhtm1Chg/Shhtm2Amc,Nkx2-5tm1(cre)Rjs/Nkx2-5+ Genetic Background: involves: 129S1/Sv * 129S7/SvEvBrd * 129X1/SvJ
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MP:0002989 | small kidney | "reduced physical bulk one or both of the organs responsible for urine secretion" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
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Allelic Composition: Smn1tm5(Smn1/SMN2)Mrph/Smn1tm5(Smn1/SMN2)Mrph Genetic Background: FVB.129(B6)-Smn1tm5(Smn1/SMN2)Mrph/J
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MP:0002990 | short ureter | "reduced length of the tube that conducts the urine from the renal pelvis to the bladder" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8] |
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Allelic Composition: Smn1tm5(Smn1/SMN2)Mrph/Smn1tm5(Smn1/SMN2)Mrph Genetic Background: FVB.129(B6)-Smn1tm5(Smn1/SMN2)Mrph/J
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MP:0003054 | spina bifida | "common congenital midline defect of fusion of the vertebral arch" [MeSH:National Library of Medicine - Medical Subject Headings, 2003] |
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Allelic Composition: Shhtm1Chg/Shhtm1Chg,Tulp3hhkr/Tulp3hhkr Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C3H/HeH * C57BL/6
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MP:0003069 | abnormal superior semicircular canal | "anomaly of the upper, superior segment of the long bony tube of the labyrinth that is involved in the sense of balance" [Stedman s Medical Dictionary, 27th edition:ISBN 0-683-40008-8, ava:Anna V. Anagnostopoulos, Mouse Genome Informatics Curator] |
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Allelic Composition: Mdm2tm1Bay/Mdm2tm1Bay,Trp53tm1Snj/Trp53tm1Snj Genetic Background: involves: C57BL/6
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MP:0003078 | aphakia | "absence of the crystalline lens of the eye" [Stedman s Medical Dictionary, 27th edition:ISBN 0-683-40008-8, ava:Anna V. Anagnostopoulos, Mouse Genome Informatics Curator] |
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Allelic Composition: Ndst1tm1.1Grob/Ndst1+,Shhtm1Chg/Shh+ Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
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MP:0003115 | abnormal respiratory system development | "aberrant differentiation of pulmonary tissues" [Stedman s Medical Dictionary, 27th edition:ISBN 0-683-40008-8] |
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Allelic Composition: Tmem107schlei/Tmem107tm1Lex Genetic Background: involves: 129S5/SvEvBrd * C3HeB/FeJ * C57BL/6J * C57BL/6N
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MP:0003120 | abnormal tracheal cartilage | "any structural anomaly of the cartilaginous structures that support the trachea" [smb:Susan M. Bello, Mouse Genome Informatics Curator, J:97123] |
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Allelic Composition: Shhtm2Amc/Shhtm2Amc,Tg(SFTPC-rtTA)5Jaw/0,Tg(tetO-cre)1Jaw/0 Genetic Background: involves: FVB/N
Allelic Composition: Shhtm1Amc/Shhtm2Amc,Tg(SFTPC-rtTA)5Jaw/0,Tg(tetO-cre)1Jaw/0 Genetic Background: involves: FVB/N
Allelic Composition: Shhtm1Amc/Shhtm1Amc Genetic Background: involves: 129/Sv * C57BL/6J * CBA/J
Allelic Composition: Yy1tm2.1Yshi/Yy1tm2.1Yshi,Shhtm1(EGFP/cre)Cjt/Shh+ Genetic Background: involves: 129S4/SvJae * C57BL/6
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MP:0003130 | anal atresia | "absence of a connection between the anal pit and the rectum" [smb:Susan M. Bello, Mouse Genome Informatics Curator, J:91491] |
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Allelic Composition: Shhtm1Amc/Shhtm1Amc Genetic Background: involves: 129/Sv * C57BL/6J * CBA/J
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MP:0003161 | absent lateral semicircular canal | |
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Allelic Composition: Mdm2tm1Bay/Mdm2tm1Bay,Trp53tm1Snj/Trp53tm1Snj Genetic Background: involves: C57BL/6
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MP:0003178 | left pulmonary isomerism | "bilaterally symmetric left lung pattern (or altered asymmetric patterning of the lung)" [smb:Susan M Bello, Mouse Genome Informatics Curator, J:93051] |
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Allelic Composition: Yy1tm2.1Yshi/Yy1tm2.1Yshi,Shhtm1(EGFP/cre)Cjt/Shh+ Genetic Background: involves: 129S4/SvJae * C57BL/6
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MP:0003189 | fused joints | |
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Allelic Composition: ShhDsh/Shh+ Genetic Background: B10Rl.Cg-ShhDsh
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MP:0003244 | loss of dopaminergic neurons | "loss of the neurons that utilize dopamine as a neurotransmitter, commonly due to an apoptotic event" [RGD:Rat Genome Database submission] |
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Allelic Composition: Shhtm1Ahk/Shhtm1Ahk,Slc6a3tm1(cre)Xz/Slc6a3+ Genetic Background: involves: 129S1/Sv * C57BL/6
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MP:0003271 | abnormal duodenum morphology | "malformation in the first division of the small intestine that extends from the pyloris to the junction with the jejunum " [MeSH:National Library of Medicine - Medical Subject Headings , 2003] |
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Allelic Composition: Shhtm1Amc/Shhtm1Amc Genetic Background: involves: 129/Sv * C57BL/6J * CBA/J
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MP:0003283 | abnormal digestive organ placement | "different location or arrangement of any of the alimentary tract organs" [ncbi:Matthew Mailman, NCBI request] |
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Allelic Composition: Shhtm1Amc/Shhtm1Amc Genetic Background: involves: 129/Sv * C57BL/6J * CBA/J
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MP:0003321 | tracheoesophageal fistula | "an abnormal passage between the esophagus and the trachea, acquired or congenital, often associated with esophageal atresia" [MeSH:National Library of Medicine - Medical Subject Headings , 2003, ncbi:Matthew Mailman, NCBI request] |
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Allelic Composition: Ednratm1Ywa/Ednratm1Ywa Genetic Background: involves: 129S7/SvEvBrd
Allelic Composition: Shhtm1Amc/Shhtm1Amc Genetic Background: involves: 129/Sv * C57BL/6J * CBA/J
Allelic Composition: Ctnnb1tm1Mmt/Ctnnb1tm1Mmt,Shhtm1(EGFP/cre)Cjt/Shh+ Genetic Background: involves: 129X1/SvJ
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MP:0003345 | decreased number of ribs | "fewer than normal numbers of the pairs of bony structures that make up the body wall" [MeSH:National Library of Medicine - Medical Subject Headings , 2003, ncbi:Matthew Mailman, NCBI request] |
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Allelic Composition: Fgfr2tm1.1Dsn/Fgfr2+ Genetic Background: involves: 129P2/OlaHsd * C57BL/6
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MP:0003424 | premature neuronal precursor differentiation | "earlier than normal transformation of neuronal precursor cells into neurons" [smb:Susan M Bello, Mouse Genome Informatics Curator, J:94391] |
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Allelic Composition: Wnt1tm1.1Mze/Wnt1tm1.1Mze,Gt(ROSA)26Sortm14(CAG-tdTomato)Hze/Gt(ROSA)26Sor+,Shhtm1(EGFP/cre)Cjt/Shh+ Genetic Background: involves: 129S6/SvEvTac * C57BL/6N
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MP:0003425 | abnormal optic vesicle formation | "anomalous formation of the hollow outgrowth from the lateral aspects of the embryonic forebrain from which the retina and optic nerve develop" [smb:Susan M Bello, Mouse Genome Informatics Curator, J:94391] |
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Allelic Composition: Fgfr2tm1.1Dsn/Fgfr2+ Genetic Background: involves: 129P2/OlaHsd * C57BL/6
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MP:0003446 | renal hypoplasia | "decreased cell number in the kidney leading to reduced size" [llw2:Linda Washburn , Mouse Genome Informatics Curator] |
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Allelic Composition: Smn1tm5(Smn1/SMN2)Mrph/Smn1tm5(Smn1/SMN2)Mrph Genetic Background: FVB.129(B6)-Smn1tm5(Smn1/SMN2)Mrph/J
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MP:0003451 | absent olfactory bulb | "absence of the forebrain region that coordinates neuronal signaling involved in the perception of smell; it receives input from the sensory neurons and outputs to the olfactory cortex" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8] |
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Allelic Composition: Shhtm2Chg/Shh+,Edil3Tg(Sox2-cre)1Amc/Edil3+ Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA
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MP:0003626 | kidney medulla hypoplasia | |
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Allelic Composition: Smn1tm5(Smn1/SMN2)Mrph/Smn1tm5(Smn1/SMN2)Mrph Genetic Background: FVB.129(B6)-Smn1tm5(Smn1/SMN2)Mrph/J
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MP:0003632 | abnormal nervous system morphology | |
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Allelic Composition: Shhtm3(cre)Chg/Shhtm3(cre)Chg Genetic Background: Not Specified
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MP:0003634 | abnormal glia | "malformation or absence of non-neuronal cells of the nervous system that form the myelin insulation of nervous pathways, guide neuronal migration during development, and exchange metabolites with neurons" [MeSH:National Library of Medicine - Medical Subject Headings , 2003] |
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Allelic Composition: Shhtm1Amc/Shhtm2Amc,Tg(Thy1-cre)703Vaw/? Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C3H * C57BL/6
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MP:0003641 | small lung | "reduced size of the lung relative to normal" [smb:Susan M Bello, Mouse Genome Informatics Curator, J:95332] |
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Allelic Composition: Gt(ROSA)26Sortm1(tetO-Sox9)Msan/Gt(ROSA)26Sortm1(rtTA,EGFP)Nagy,Shhtm1(EGFP/cre)Cjt/Shh+ Genetic Background: involves: 129S1/Sv * 129X1/SvJ
Allelic Composition: Sox9tm1Gsr/Sox9tm1Gsr,Shhtm1(EGFP/cre)Cjt/Shh+ Genetic Background: involves: 129P2/OlaHsd
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MP:0003672 | abnormal ureter development | "anomalous differentiation of the tube that conducts the urine from the renal pelvis to the bladder" [smb:Susan M Bello, Mouse Genome Informatics Curator, J:96485] |
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Allelic Composition: Smn1tm5(Smn1/SMN2)Mrph/Smn1tm5(Smn1/SMN2)Mrph Genetic Background: FVB.129(B6)-Smn1tm5(Smn1/SMN2)Mrph/J
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MP:0003704 | abnormal hair follicle development | "anomalous development of the epidermis from which the hair shaft develops " [monikat:Monika Tomczuk, Mouse Genome Informatics Curator] |
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Allelic Composition: Shhtm1Amc/Shhtm1Amc Genetic Background: involves: 129/Sv * C57BL/6J * CBA/J
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MP:0003710 | abnormal physiological neovascularization | "anomalies in the development of new blood vessels in restoration of blood circulation during the healing process " [MeSH:National Library of Medicine - Medical Subject Headings , 2003] |
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Allelic Composition: Brca2tm1Brn/Brca2tm1Brn,Trp53bp1tm1Jc/Trp53bp1tm1Jc,Cd19tm1(cre)Cgn/Cd19+ Genetic Background: involves: 129P2/OlaHsd
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MP:0003723 | abnormal long bone morphology | "malformation of any of the several elongated bones of the extremities
" [monikat:Monika Tomczuk, Mouse Genome Informatics Curator] |
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Allelic Composition: Fgfr2tm1.1Dsn/Fgfr2+ Genetic Background: involves: 129P2/OlaHsd * C57BL/6
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MP:0003743 | abnormal facial morphology | "anomalous structure or development of the face" [ncbi:Matthew Mailman, NCBI request] |
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Allelic Composition: Disp1tm2.1Amc/Disp1tm2Amc,Shhtm1(EGFP/cre)Cjt/Shh+ Genetic Background: involves: 129/Sv * C57BL/6J * SWR
Allelic Composition: Disp1icb/Disp1tm2Amc,Shhtm1(EGFP/cre)Cjt/Shh+ Genetic Background: involves: 129/Sv * C57BL/6J * SWR
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MP:0003793 | abnormal submandibular gland morphology | "any structural malformation of either of the large major salivary glands situated beneath the mandible" [anna:Anna Anagnostopoulos, Mouse Genome Informatics Curator] |
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Allelic Composition: Zfpm1tm2Sho/Zfpm1tm2Sho Genetic Background: either: (involves: 129S1/Sv) or (involves: 129S1/Sv * C57BL/6)
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MP:0003809 | abnormal hair shaft morphology | "irregular or unusual structure of the cuticle, and/or cortex and/or medulla of a hair" [llw2:Linda Washburn , Mouse Genome Informatics Curator] |
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Allelic Composition: Shhtm1Amc/Shhtm1Amc Genetic Background: involves: 129/Sv * C57BL/6J * CBA/J
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MP:0003855 | abnormal forelimb zeugopod morphology | |
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Allelic Composition: Shhtm1Chg/Shhtm1Chg Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
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MP:0003857 | abnormal hindlimb zeugopod morphology | |
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Allelic Composition: Shhtm1Chg/Shhtm1Chg Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
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MP:0003885 | abnormal rostro-caudal body axis extension | "anomaly in or failure of the long (rostral-caudal) axis of the body to elongate normally once patterning has been established" [brs:Beverly Richards-Smith, Mouse Genome Informatics Curator] |
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Allelic Composition: Gas1tm2Fan/Gas1tm2Fan,Shhtm1Chg/Shhtm1Chg Genetic Background: involves: 129/Sv * 129S1/Sv * 129X1/SvJ * C57BL/6J
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MP:0003923 | abnormal left atrium morphology | "structural anomaly of the left upper chamber of the heart " [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
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Allelic Composition: Lamp1tm1Psa/Lamp1tm1Psa,Lamp2tm1Psa/Y Genetic Background: involves: 129P2/OlaHsd * C57BL/6
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MP:0003936 | abnormal reproductive system development | "developmental anomaly of any of the organs involved in the reproductive system" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
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Allelic Composition: Gt(ROSA)26Sortm1(Fgf8)Lma/Gt(ROSA)26Sor+,Tg(Msx2-cre)5Rem/0 Genetic Background: involves: C57BL/6 * CBA
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MP:0003961 | decreased lean body mass | "less than average fat-free physical bulk or volume of the body including all its components except adipose tissue" [honda:Hiraoki Onda, Mouse GEnome Informatics Curator] |
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Allelic Composition: Setxtm1b(EUCOMM)Wtsi/Setxtm1b(EUCOMM)Wtsi Genetic Background: C57BL/6N-Setxtm1b(EUCOMM)Wtsi/Ics
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MP:0003984 | embryonic growth retardation | "slow or limited development before birth" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
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Allelic Composition: Shhtm1Chg/Shhtm1Chg Genetic Background: involves: C57BL/6
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MP:0004007 | abnormal lung vasculature | "malformation or disorganization of the blood vessels of the lung" [smb:Susan M Bello, Mouse Genome Informatics Curator] |
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Allelic Composition: Shhtm1Amc/Shhtm1Amc Genetic Background: involves: 129/Sv * C57BL/6J * CBA/J
Allelic Composition: Ctnnb1tm1Mmt/Ctnnb1tm1Mmt,Shhtm1(EGFP/cre)Cjt/Shh+ Genetic Background: involves: 129X1/SvJ
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MP:0004098 | abnormal granule neuron | "any structural anomaly of the small neurons of the granule cell layer that send parallel fibers to the upper molecular layer, where they synapse with Purkinje cell dendrites" [Principles of Neural Science , 3rd edition:ISBN 0-8385-8034-3] |
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Allelic Composition: Shhtm2Amc/Shhtm3Amc,Tg(Pax2-cre)1Amc/0 Genetic Background: involves: 129S1/Sv * 129X1/SvJ * Black Swiss
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MP:0004100 | abnormal spinal cord interneuron morphology | "malformation or absence of neurons that exclusively interact with other neurons in the spinal cord" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
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Allelic Composition: Fgfr2tm1.1Dsn/Fgfr2+ Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Allelic Composition: Gli2tm2.1Alj/Gli2tm2.1Alj,Shhtm1Chg/Shhtm1Chg Genetic Background: either: (involves: 129) or (involves: 129 * Black Swiss)
Allelic Composition: Shhtm1Ptch/Shhtm1Ptch Genetic Background: involves: 129P2/OlaHsd * FVB/N * various
Allelic Composition: Gli2tm2.1Alj/Gli2tm3.1(Gli1)Alj,Shhtm1Chg/Shhtm1Chg Genetic Background: either: (involves: 129) or (involves: 129 * Black Swiss)
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MP:0004101 | abnormal brain interneuron morphology | "malformation or absence of neurons that exclusively interact with other neurons in the brain; this includes most brain neuronal cell types" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
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Allelic Composition: Shhtm2Amc/Shhtm2Amc,Tg(Nes-cre)1Kln/0 Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL
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MP:0004137 | abnormal gastric surface mucous cells | "malformation of the mucus secreting epithelial cells that lline the luminal surface of the stomach, gastric pits and gastric glands" [monikat:Monika Tomczuk, Mouse Genome Informatics Curator] |
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Allelic Composition: Brca2tm1Brn/Brca2tm1Brn,Trp53bp1tm1Jc/Trp53bp1tm1Jc,Cd19tm1(cre)Cgn/Cd19+ Genetic Background: involves: 129P2/OlaHsd
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MP:0004173 | abnormal intervertebral disk morphology | "malformation of the cartilagenous and gelatinous structure found between vertebrae" [smb:Susan M Bello, Mouse Genome Informatics Curator] |
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Allelic Composition: Gas1tm2Fan/Gas1tm2Fan,Shhtm1Chg/Shh+ Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6J
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MP:0004180 | failure of initiation of embryo turning | "failure to begin the axial rotation of the germ layers of the embryo during the primitive streak/early somite stage (E8.5-E9.5)" [monikat:Monika Tomczuk, Mouse Genome Informatics Curator] |
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Allelic Composition: Tyrc-32DSD/Tyrc Genetic Background: involves: 101/Rl * C3H/Rl
Allelic Composition: Shhtm1Chg/Shhtm1Chg,Zic2Ku/Zic2Ku Genetic Background: involves: 129S1/Sv * 129X1/SvJ * BALB/cAnNCrl * C3H/HeH
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MP:0004196 | abnormal prenatal growth/weight/body size | "limited or accelerated growth or development apparent before birth" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Shhtm3(cre)Chg/Shhtm3(cre)Chg Genetic Background: Not Specified
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MP:0004200 | reduced fetal size | "smaller proportions of a fetus compared to littermates (sensu Mus: from E14 through birth)" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Shhtm1Amc/Shhtm1Amc Genetic Background: involves: 129/Sv * C57BL/6J * CBA/J
Allelic Composition: Gas1tm2Fan/Gas1tm2Fan,Shhtm1Chg/Shh+ Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6J
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MP:0004201 | fetal growth retardation | "slow or limited development during the fetal period (sensu Mus: from E14 through birth)" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Fgfr2tm1.1Dsn/Fgfr2+ Genetic Background: involves: 129P2/OlaHsd * C57BL/6
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MP:0004251 | failure of looping morphogenesis | "failure of the primitive heart tube to initiate or complete looping" [MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator"] |
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Allelic Composition: Disp1icb/Disp1tm1Amc,Shhtm1Amc/Shh+ Genetic Background: involves: 129X1/SvJ * C57BL/6J
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MP:0004268 | abnormal optic stalk morphology | "any structural anomaly of the narrow, proximal portion of the optic vesicle which connects the embryonic eye and forebrain" [ISBN:0-914294-08-3 "Gray s Anatomy"] |
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Allelic Composition: Fgfr2tm1.1Dsn/Fgfr2+ Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Allelic Composition: Six3tm3.1Gco/Six3+,Shhtm1Chg/Shh+ Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
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MP:0004269 | abnormal optic cup morphology | "any structural anomaly of double walled stuctured formed by expansion and invagination of the distal end of the optic vesicle that develops into the pigmented and sensory layers of the retina while the mouth of the optic cup eventually forms the pupil of the eye" [MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator"] |
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Allelic Composition: Fgfr2tm1.1Dsn/Fgfr2+ Genetic Background: involves: 129P2/OlaHsd * C57BL/6
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MP:0004274 | abnormal embryonic/fetal subventricular zone morphology | "any structural anomaly in the transient proliferative population of neurons that expands exponentially during late prenatal development; it is a continuous germinal zone distinct from the ventricular zone that surrounds the brain ventricles" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator", PMID:12637172] |
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Allelic Composition: Shhtm2Chg/Shh+,Edil3Tg(Sox2-cre)1Amc/Edil3+ Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA
Allelic Composition: Shhtm1.1Rseg/Shhtm1.1Rseg Genetic Background: involves: 129S4/SvJae * C57BL/6
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MP:0004275 | abnormal postnatal subventricular zone morphology | "any structural anomaly of the mitotically active layer of cells surrounding the brain ventricles in the adult that consists of migrating neuroblasts, astrocytes and transitory amplifying progenitor cells" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator", PMID:12637172] |
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Allelic Composition: Shhtm1.1Rseg/Shhtm1.1Rseg Genetic Background: involves: 129S4/SvJae * C57BL/6
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MP:0004276 | abnormal medial ganglionic eminence morphology | "any structural anomaly of a distinct elevation of a transient proliferating cell mass of the fetal subventricular zone; this mass contributes most of its cells to the neocortex; however, hippocampal neurons, thalamus, septum and olfactory bulb neurons are also partly derived from the MGE" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator", PMID:12637172] |
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Allelic Composition: Shhtm2Amc/Shhtm2Amc,Tg(Nes-cre)1Kln/0 Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL
Allelic Composition: Shhtm2Chg/Shh+,Edil3Tg(Sox2-cre)1Amc/Edil3+ Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA
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MP:0004277 | abnormal lateral ganglionic eminence morphology | "any structural anomaly of a distinct elevation of a transient proliferating cell mass of the fetal subventricular zone; this mass contributes most of its cells to the striatum; however, neocortex, thalamus, septum and olfactory bulb neurons are also partly derived from the LGE" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator", PMID:12637172] |
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Allelic Composition: Shhtm2Chg/Shh+,Edil3Tg(Sox2-cre)1Amc/Edil3+ Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA
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MP:0004313 | absent vestibulocochlear ganglion | "absence of the group of neuron cell bodies associated with the eighth cranial nerve during embryogenesis; splits in later development to form the cochlear and vestibular ganglia" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"] |
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Allelic Composition: Mdm2tm1Bay/Mdm2tm1Bay,Trp53tm1Snj/Trp53tm1Snj Genetic Background: involves: C57BL/6
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MP:0004315 | absent saccule | "absence of the smaller of the two sacs in the vestibule " [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"] |
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Allelic Composition: Mdm2tm1Bay/Mdm2tm1Bay,Trp53tm1Snj/Trp53tm1Snj Genetic Background: involves: C57BL/6
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MP:0004354 | absent deltoid tuberosity | "missing the rough elevation at the middle of the lateral side of the shaft of the humerus to which the deltoid muscle attaches" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"] |
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Allelic Composition: Ccd/Ccd+,ShhDsh/Shh+ Genetic Background: involves: 101 * C3H * C57BL * C57BL/10Rl * SEC
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MP:0004358 | bowed tibia | "increased curvature of the medial and larger of the two bones of the lower leg" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"] |
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Allelic Composition: ShhDz/ShhDz Genetic Background: C57BL/6J-ShhDz
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MP:0004369 | absent utricle | "absence of the larger of the two sacs in the vestibule" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Mdm2tm1Bay/Mdm2tm1Bay,Trp53tm1Snj/Trp53tm1Snj Genetic Background: involves: C57BL/6
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MP:0004372 | bowed fibula | "increased curvature of the lateral and smaller bone of the lower limb" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"] |
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Allelic Composition: ShhDz/ShhDz Genetic Background: C57BL/6J-ShhDz
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MP:0004391 | abnormal respiratory conducting tube | "any structural anomaly of the tubes of the respiratory system that allows passage of air from the trachea to the alveoli of the lungs" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Lamp1tm1Psa/Lamp1tm1Psa,Lamp2tm1Psa/Y Genetic Background: involves: 129P2/OlaHsd * C57BL/6
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MP:0004419 | absent parietal bone | "absence of the curved bone forming part of the vault of the cranium" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Disp1icb/Disp1tm2Amc,Shhtm1(EGFP/cre)Cjt/Shh+ Genetic Background: involves: 129/Sv * C57BL/6J * SWR
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MP:0004423 | abnormal squamosal bone morphology | "any structural anomaly of the thin, platelike part of the temporal bone" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Ccd/Ccd+,ShhDsh/Shh+ Genetic Background: involves: 101 * C3H * C57BL * C57BL/10Rl * SEC
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MP:0004442 | occipital bone foramen | "presence of a hole in the bone at the lower, posterior part of the skull" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"] |
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Allelic Composition: ShhDsh/Shh+ Genetic Background: B10Rl.Cg-ShhDsh
Allelic Composition: Ccd/Ccd+,ShhDsh/Shh+ Genetic Background: involves: 101 * C3H * C57BL * C57BL/10Rl * SEC
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MP:0004473 | absent nasal bone | "absence of either of two rectangular bone plates forming the bridge of the nose" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"] |
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Allelic Composition: Ccd/Ccd+,ShhDsh/Shh+ Genetic Background: involves: 101 * C3H * C57BL * C57BL/10Rl * SEC
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MP:0004505 | decreased renal glomerulus number | "reduced number of the capillary loops of the kidney that normally function as a filtration unit" [MGI:monikat "Monika Tomczuk, Mouse Genome Informatics Curator"] |
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Allelic Composition: Smn1tm5(Smn1/SMN2)Mrph/Smn1tm5(Smn1/SMN2)Mrph Genetic Background: FVB.129(B6)-Smn1tm5(Smn1/SMN2)Mrph/J
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MP:0004506 | abnormal pubic bone morphology | "any structural anomaly in the forward portion of either of the hipbones, at the juncture forming the front arch of the pelvis" [MGI:monikat "Monika Tomczuk, Mouse Genome Informatics Curator"] |
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Allelic Composition: Ccd/Ccd+,ShhDsh/Shh+ Genetic Background: involves: 101 * C3H * C57BL * C57BL/10Rl * SEC
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MP:0004507 | abnormal ischium morphology | "any structural anomaly of the lowest of the three major bones that constitute each half of the pelvis, distinct at birth but later becoming fused with the ilium and pubis" [MGI:monikat "Monika Tomczuk, Mouse Genome Informatics Curator"] |
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Allelic Composition: Ccd/Ccd+,ShhDsh/Shh+ Genetic Background: involves: 101 * C3H * C57BL * C57BL/10Rl * SEC
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MP:0004508 | abnormal shoulder bone morphology | "any structural anomaly of the bones of the shoulder by which the limbs attach to the axial skeleton " [MGI:cwg "Carroll-Ann W. Goldsmith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Ccd/Ccd+,ShhDsh/Shh+ Genetic Background: involves: 101 * C3H * C57BL * C57BL/10Rl * SEC
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MP:0004509 | abnormal pelvic girdle bone morphology | "any structural anomaly of the bones of the pelvis by which the limbs attach to the axial skeleton " [MGI:cwg "Carroll-Ann W. Goldsmith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Ccd/Ccd+,ShhDsh/Shh+ Genetic Background: involves: 101 * C3H * C57BL * C57BL/10Rl * SEC
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MP:0004538 | abnormal maxillary shelf | "any structural anomaly of the outgrowth of the maxilla that normally fuses with palatine shelf to form secondary (hard) palate" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition", MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Shhtm2Chg/Shh+,Edil3Tg(Sox2-cre)1Amc/Edil3+ Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA
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MP:0004551 | decreased tracheal cartilage ring number | "less than the 16-20 incomplete rings of hyaline cartilage forming the skeleton of the trachea" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"] |
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Allelic Composition: Shhtm2Amc/Shhtm2Amc,Tg(SFTPC-rtTA)5Jaw/0,Tg(tetO-cre)1Jaw/0 Genetic Background: involves: FVB/N
Allelic Composition: Shhtm1Amc/Shhtm2Amc,Tg(SFTPC-rtTA)5Jaw/0,Tg(tetO-cre)1Jaw/0 Genetic Background: involves: FVB/N
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MP:0004553 | absent tracheal cartilage rings | "absence of the 16-20 incomplete rings of hyaline cartilage forming the skeleton of the trachea" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"] |
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Allelic Composition: Ednratm1Ywa/Ednratm1Ywa Genetic Background: involves: 129S7/SvEvBrd
Allelic Composition: Shhtm1Amc/Shhtm1Amc,Tg(SFTPC-rtTA)5Jaw/0,Tg(tetO-Shh)1Jaw/0 Genetic Background: involves: FVB/N
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MP:0004576 | abnormal foot plate morphology | "any structural anomaly of the distal elements of the developing limb of vertebrates that will give rise to the pedal appendages (e.g. hand, foot, paw)" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Fgfr1tm3.2Cxd/Fgfr1tm3.2Cxd,Shhtm1(EGFP/cre)Cjt/Shh+ Genetic Background: involves: 129S6/SvEvTac
Allelic Composition: Fgfr1tm3.1Cxd/Fgfr1tm3.2Cxd,Shhtm1(EGFP/cre)Cjt/Shh+ Genetic Background: involves: 129S6/SvEvTac
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MP:0004620 | cervical vertebral fusion | "the union of one or more cervical vertebrae into a single structure" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: ShhDsh/Shh+ Genetic Background: B10Rl.Cg-ShhDsh
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MP:0004634 | short metacarpal bones | "reduced length of the five bones of the forepaws that articulate proximally with the carpal bones and distally with the phalanges" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"] |
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Allelic Composition: ShhDsh/Shh+ Genetic Background: B10Rl.Cg-ShhDsh
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MP:0004658 | abnormal ventral tubercle of atlas | "any structural anomaly of the conical ventral projection on the arch of the atlas" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Ccd/Ccd+,ShhDsh/Shh+ Genetic Background: involves: 101 * C3H * C57BL * C57BL/10Rl * SEC
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MP:0004712 | notochord degeneration | "retrogressive pathologic change of the axial fibrocellular cord in embryos around which develops the vertebral primordia (prior to normal differentiation of this tissue into the vertebral column tissues)" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"] |
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Allelic Composition: Fgfr2tm1.1Dsn/Fgfr2+ Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Allelic Composition: Shhtm1Amc/Shhtm1Amc Genetic Background: involves: 129S1/Sv * 129X1/SvJ
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MP:0004872 | absent nasal septum | "absence of the structure that separates the two nasal cavities" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"] |
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Allelic Composition: Six3tm3.1Gco/Six3+,Shhtm1Chg/Shh+ Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
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MP:0004880 | lung cysts | |
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Allelic Composition: Shhtm2Amc/Shhtm2Amc,Tg(SFTPC-rtTA)5Jaw/0,Tg(tetO-cre)1Jaw/0 Genetic Background: involves: FVB/N
Allelic Composition: Shhtm1Amc/Shhtm2Amc,Tg(SFTPC-rtTA)5Jaw/0,Tg(tetO-cre)1Jaw/0 Genetic Background: involves: FVB/N
Allelic Composition: Gt(ROSA)26Sortm1(tetO-Sox9)Msan/Gt(ROSA)26Sortm1(rtTA,EGFP)Nagy,Shhtm1(EGFP/cre)Cjt/Shh+ Genetic Background: involves: 129S1/Sv * 129X1/SvJ
Allelic Composition: Sox9tm1Gsr/Sox9tm1Gsr,Shhtm1(EGFP/cre)Cjt/Shh+ Genetic Background: involves: 129P2/OlaHsd
Allelic Composition: Dicer1tm1Mmk/Dicer1tm1Mmk,Shhtm1(EGFP/cre)Cjt/Shh+ Genetic Background: involves: 129 * C57BL/6J
Allelic Composition: Yy1tm2.1Yshi/Yy1tm2.1Yshi,Shhtm1(EGFP/cre)Cjt/Shh+ Genetic Background: involves: 129S4/SvJae * C57BL/6
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MP:0004882 | enlarged lung | "increased size of the lung compared to controls" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Dicer1tm1Mmk/Dicer1tm1Mmk,Shhtm1(EGFP/cre)Cjt/Shh+ Genetic Background: involves: 129 * C57BL/6J
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MP:0004980 | increased neuronal precursor cell number | "increased number of the neuroblast embryonic cells that develop into nerve cells or neurons" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Gas1tm2Fan/Gas1tm2Fan,Shhtm1Chg/Shh+ Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6J
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MP:0004981 | decreased neuronal precursor cell number | "reduced number of the neuroblast embryonic cells that develop into nerve cells or neurons" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Gas1tm2Fan/Gas1tm2Fan,Shhtm1Chg/Shh+ Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6J
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MP:0005076 | abnormal cell differentiation | "anomaly in the process whereby relatively unspecialized cells, e. g. embryonic or regenerative cells, acquire specialized structural and/or functional features that characterize the cells, tissues, or organs of the mature organism or some other relatively stable phase of the organism s life history" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator] |
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Allelic Composition: Sox9tm1Gsr/Sox9tm1Gsr,Shhtm1(EGFP/cre)Cjt/Shh+ Genetic Background: involves: 129P2/OlaHsd
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MP:0005084 | abnormal gall bladder morphology | "anomalous structure or development of the organ which serves as a storage reservoir for bile" [Stedman s Medical Dictionary:ISBN 0-683-40008-8] |
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Allelic Composition: Lamp1tm1Psa/Lamp1tm1Psa,Lamp2tm1Psa/Y Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Allelic Composition: Shhtm1(EGFP/cre)Cjt/Shh+,Sox17tm1Ysk/Sox17+ Genetic Background: involves: 129S1/Sv * C57BL/6
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MP:0005104 | abnormal tarsus morphology | "malformation or absence of any of the eight bones of the instep of the paw: tibiale, talus, calcaneus, navicular, 3 cuneiform, and cuboid bones" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:83132, Anatomy of the Rat:Greene, EC, Hafner Publishing Co, 1935] |
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Allelic Composition: Cd19tm1(cre)Cgn/Cd19+,Gt(ROSA)26Sortm4(Ikbkb)Rsky/Gt(ROSA)26Sor+ Genetic Background: involves: 129P2/OlaHsd * C57BL/6
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MP:0005157 | holoprosencephaly | "presence of a single forebrain hemisphere or lobe; often accompanied by a deficit in median facial development" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:83058] |
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Allelic Composition: Shhtm1Chg/Shhtm1Chg Genetic Background: involves: C57BL/6
Allelic Composition: Shhtm1Ptch/Shhtm1Ptch Genetic Background: involves: 129P2/OlaHsd * FVB/N * various
Allelic Composition: Disp1icb/Disp1tm1Amc,Shhtm1Amc/Shh+ Genetic Background: involves: 129X1/SvJ * C57BL/6J
Allelic Composition: Shhtm2Chg/Shh+,Edil3Tg(Sox2-cre)1Amc/Edil3+ Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA
Allelic Composition: Gas1tm2Fan/Gas1tm2Fan,Shhtm1Chg/Shh+ Genetic Background: involves: 129/Sv * 129S1/Sv * 129X1/SvJ * C57BL/6J
Allelic Composition: Shhtm1Amc/Shhtm1Amc Genetic Background: involves: 129S1/Sv * 129X1/SvJ
Allelic Composition: Shhtm1Amc/Shhtm2Amc,Tg(Thy1-cre)703Vaw/? Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C3H * C57BL/6
Allelic Composition: Six3tm3.1Gco/Six3+,Shhtm1Chg/Shh+ Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
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MP:0005163 | cyclopia | "a congenital defect in which the two orbits are united to form a single cavity containing one eye" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:60303] |
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Allelic Composition: Fgfr2tm1.1Dsn/Fgfr2+ Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Allelic Composition: Gli2tm2.1Alj/Gli2tm2.1Alj,Shhtm1Chg/Shhtm1Chg Genetic Background: either: (involves: 129) or (involves: 129 * Black Swiss)
Allelic Composition: Shhtm1Chg/Shhtm1Chg Genetic Background: involves: C57BL/6
Allelic Composition: Shhtm1(EGFP/cre)Cjt/Shhtm2Amc Genetic Background: involves: 129/Sv * C57BL/6J * SWR
Allelic Composition: ShhDsh/ShhDsh Genetic Background: involves: 101 * C3H * C57BL * SEC
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MP:0005213 | gastric metaplasia | "condition in which there is a change of one adult cell type to another adult cell type in the stomach " [MeSH:National Library of Medicine - Medical Subject Headings , 2003, J:77398] |
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Allelic Composition: Shhtm1Amc/Shhtm1Amc Genetic Background: involves: 129/Sv * C57BL/6J * CBA/J
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MP:0005293 | impaired glucose tolerance | "less than the normal response to oral consumption or intravenous injection of specified amounts of glucose and indicative of insulin resistance; measured by determining whole blood or plasma sugar level in a fasting state before and after taking glucose at specified intervals" [MeSH:National Library of Medicine - Medical Subject Headings , 2003] |
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Allelic Composition: Setxtm1b(EUCOMM)Wtsi/Setxtm1b(EUCOMM)Wtsi Genetic Background: C57BL/6N-Setxtm1b(EUCOMM)Wtsi/Ics
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MP:0005296 | abnormal humerus morphology | "malformation of the bone of the forelimb that articulates with the scapula above and the radius and ulna below" [Stedman s Medical Dictionary:ISBN 0-683-40008-8] |
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Allelic Composition: Fgfr2tm1.1Dsn/Fgfr2+ Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Allelic Composition: Ccd/Ccd+,ShhDsh/Shh+ Genetic Background: involves: 101 * C3H * C57BL * C57BL/10Rl * SEC
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MP:0005298 | abnormal clavicle morphology | "malformation of the doubly curved long bone that forms part of the shoulder girdle and articulates with the sternum and the scapula" [Stedman s Medical Dictionary:ISBN 0-683-40008-8] |
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Allelic Composition: Ccd/Ccd+,ShhDsh/Shh+ Genetic Background: involves: 101 * C3H * C57BL * C57BL/10Rl * SEC
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MP:0005306 | abnormal phalanx morphology | "aberrant structure of any of the long bones of the digits" [Stedman s Medical Dictionary:ISBN 0-683-40008-8] |
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Allelic Composition: ShhDsh/Shh+ Genetic Background: B10Rl.Cg-ShhDsh
Allelic Composition: Gli3tm2Blnw/Gli3+,Shhtm1Chg/Shhtm1Chg Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N
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MP:0005325 | abnormal glomerulus | "anomalous structure of the capillary loops of the kidney that normally function as a filtration unit" [J:57971, cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator] |
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Allelic Composition: Smn1tm5(Smn1/SMN2)Mrph/Smn1tm5(Smn1/SMN2)Mrph Genetic Background: FVB.129(B6)-Smn1tm5(Smn1/SMN2)Mrph/J
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MP:0005358 | abnormal incisor morphology | "structural defect of the long pointed teeth; most anterior and prominent in the jaw" [pvb:Pierre Vanden Borre , Mouse Genome Informatics Curator, J:85574] |
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Allelic Composition: Shhtm1Amc/Shhtm2Amc,Tg(KRT14-cre)1Amc/0 Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA
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MP:0005359 | growth retardation of incisors | "developmental delay of the growth of the incisors, the long pointed teeth, most anterior and prominent in the jaw " [pvb:Pierre Vanden Borre , Mouse Genome Informatics Curator, J:85574] |
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Allelic Composition: Shhtm1Amc/Shhtm2Amc,Tg(KRT14-cre)1Amc/0 Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA
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MP:0005430 | absent fibula | "missing the lateral and shorter of the two bones of the lower leg" [pvb:Pierre Vanden Borre , Mouse Genome Informatics Curator, J:86196] |
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Allelic Composition: Fgfr2tm1.1Dsn/Fgfr2+ Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Allelic Composition: ShhDz/ShhDz Genetic Background: C57BL/6J-ShhDz
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MP:0005493 | stomach epithelial hyperplasia | |
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Allelic Composition: Shhtm1Amc/Shhtm1Amc Genetic Background: involves: 129/Sv * C57BL/6J * CBA/J
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MP:0005508 | abnormal skeleton morphology | "malformation of the bony framework of the body in vertebrates" [Stedman s Medical Dictionary:ISBN 0-683-40008-8] |
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Allelic Composition: Shhtm3(cre)Chg/Shhtm3(cre)Chg Genetic Background: Not Specified
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MP:0005592 | abnormal vascular smooth muscle morphology | "structural anomaly of the nonstriated, involuntary muscle tissue of the blood vessels" [MeSH:National Library of Medicine - Medical Subject Headings , 2003, cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator] |
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Allelic Composition: Lamp1tm1Psa/Lamp1tm1Psa,Lamp2tm1Psa/Y Genetic Background: involves: 129P2/OlaHsd * C57BL/6
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MP:0005621 | abnormal cell physiology | "aberration in the vital processes of the cell " [Stedman s Medical Dictionary:ISBN 0-683-40008-8, hdene:Howard Dene , Mouse Genome Informatics Curator] |
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Allelic Composition: Shhtm3(cre)Chg/Shhtm3(cre)Chg Genetic Background: Not Specified
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MP:0005643 | decreased dopamine level | "less than the normal concentration of this catecholamine neurotransmitter, dervied from tyrosine and the precursor to norepinephrine and epinephrine" [MeSH:National Library of Medicine - Medical Subject Headings , 2003, J:88298] |
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Allelic Composition: Shhtm1Ahk/Shhtm1Ahk,Slc6a3tm1(cre)Xz/Slc6a3+ Genetic Background: involves: 129S1/Sv * C57BL/6
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MP:0005650 | abnormal limb bud morphology | "aberrant structure or development of any of the swellings on the trunk of the embryo that become limbs" [hdene:Howard Dene , Mouse Genome Informatics Curator, MeSH:National Library of Medicine - Medical Subject Headings , 2003, J:61460] |
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Allelic Composition: Gt(ROSA)26Sortm1(rtTA,EGFP)Nagy/Gt(ROSA)26Sor+,Sox9tm3(cre)Crm/Sox9+,Tg(tetO-Vegfa)1Kesh/0 Genetic Background: involves: 129S1/Sv * 129S7/SvEvBrd * 129X1/SvJ
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MP:0006030 | abnormal otic vesicle formation | "anomalous formation of the simple epithelial sac formed from the otic placode that gives rise to the structures of the inner ear" [smb:Susan M Bello, Mouse Genome Informatics Curator, J:57313:] |
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Allelic Composition: Mdm2tm1Bay/Mdm2tm1Bay,Trp53tm1Snj/Trp53tm1Snj Genetic Background: involves: C57BL/6
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MP:0006042 | increased apoptosis | "greater than normal programmed cell death" [RGD:Rat Genome Database submission, smb:Susan M Bello, Mouse Genome Informatics Curator] |
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Allelic Composition: Fgfr2tm1.1Dsn/Fgfr2+ Genetic Background: involves: 129P2/OlaHsd * C57BL/6
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MP:0006097 | abnormal cerebellar lobule formation | "anomaly in the formation of the lobes of the cerebellum" [smb:Susan M Bello, Mouse Genome Informatics Curator, anna:Anna Anagnostopoulos, Mouse Genome Informatics Curator, J:65410] |
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Allelic Composition: Ahrtm1Gonz/Ahrtm1Gonz Genetic Background: involves: 129S4/SvJae
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MP:0006098 | absent cerebellar lobules | "missing lobes of the cerebellum" [anna:Anna Anagnostopoulos, Mouse Genome Informatics Curator, smb:Susan M Bello, Mouse Genome Informatics Curator] |
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Allelic Composition: Shhtm2Amc/Shhtm3Amc,Tg(Pax2-cre)1Amc/0 Genetic Background: involves: 129S1/Sv * 129X1/SvJ * Black Swiss
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MP:0006126 | abnormal outflow tract development | "anomaly in the development of the common arterial trunk that forms the aorta and pulmonary artery" [smb:Susan M Bello, Mouse Genome Informatics Curator] |
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Allelic Composition: Shhtm1Chg/Shhtm2Amc,Nkx2-5tm1(cre)Rjs/Nkx2-5+ Genetic Background: involves: 129S1/Sv * 129S7/SvEvBrd * 129X1/SvJ
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MP:0006197 | ocular hypotelorism | "the distance between the eyes is reduced" [ncbi:Matthew Mailman, NCBI request, smb:Susan M Bello, Mouse Genome Informatics Curator] |
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Allelic Composition: Six3tm3.1Gco/Six3+,Shhtm1Chg/Shh+ Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
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MP:0006261 | annular pancreas | "an abnormal ring or collar of pancreatic tissue that encircles the duodenum" [smb:Susan M Bello, Mouse Genome Informatics Curator, J:69854] |
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Allelic Composition: Shhtm1Amc/Shhtm1Amc Genetic Background: involves: 129/Sv * C57BL/6J * CBA/J
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MP:0006279 | abnormal limb development | "anomaly in the formation of the limbs" [MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator"] |
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Allelic Composition: Fgfr2tm1.1Dsn/Fgfr2+ Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Allelic Composition: Gt(ROSA)26Sortm1(Fgf8)Lma/Gt(ROSA)26Sor+,Shhtm2(cre/ERT2)Cjt/Shhtm2(cre/ERT2)Cjt,Tg(Msx2-cre)5Rem/0 Genetic Background: involves: 129S6/SvEvTac * C57BL/6 * CBA
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MP:0006281 | abnormal tail development | "anomaly in the formation of the tail" [MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator"] |
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Allelic Composition: Gt(ROSA)26Sortm1(Fgf8)Lma/Gt(ROSA)26Sor+,Tg(Msx2-cre)5Rem/0 Genetic Background: involves: C57BL/6 * CBA
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MP:0006290 | proboscis | "a long, cylindric protuberance of the face that, in cyclopia or ethmocephaly, represents the nose" [J:92058, MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"] |
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Allelic Composition: Disp1icb/Disp1tm1Amc,Shhtm1Amc/Shh+ Genetic Background: involves: 129X1/SvJ * C57BL/6J
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MP:0006306 | abnormal nasal pit morphology | "malformation of one or both of a pair of depressions formed in the developing face that give rise to the rostral portion of the nasal meatus" [J:119812, MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator"] |
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Allelic Composition: Fgfr2tm1.1Dsn/Fgfr2+ Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Allelic Composition: Disp1tm2.1Amc/Disp1tm2Amc,Shhtm1(EGFP/cre)Cjt/Shh+ Genetic Background: involves: 129/Sv * C57BL/6J * SWR
Allelic Composition: Disp1icb/Disp1tm2Amc,Shhtm1(EGFP/cre)Cjt/Shh+ Genetic Background: involves: 129/Sv * C57BL/6J * SWR
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MP:0006382 | abnormal lung epithelium morphology | "any structural anomaly of the epithelial layer of the lung" [MGI:rbabiuk "Randall Babiuk, Mouse Genome Informatics Curator", MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator"] |
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Allelic Composition: Dicer1tm1Bdh/Dicer1tm1Bdh,Shhtm1(EGFP/cre)Cjt/Shh+ Genetic Background: involves: 129
Allelic Composition: Sox9tm1Gsr/Sox9tm1Gsr,Shhtm1(EGFP/cre)Cjt/Shh+ Genetic Background: involves: 129P2/OlaHsd
Allelic Composition: Dicer1tm1Mmk/Dicer1tm1Mmk,Shhtm1(EGFP/cre)Cjt/Shh+ Genetic Background: involves: 129 * C57BL/6J
Allelic Composition: Yy1tm2.1Yshi/Yy1tm2.1Yshi,Shhtm1(EGFP/cre)Cjt/Shh+ Genetic Background: involves: 129S4/SvJae * C57BL/6
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MP:0006402 | small molars | "reduced size of the most posterior teeth located on either side of the jaw, and characterized by a large crown and broad chewing surface" [MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator"] |
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Allelic Composition: Shhtm1Amc/Shhtm2Amc,Tg(KRT14-cre)1Amc/0 Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA
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MP:0008004 | abnormal stomach pH | "anomaly in the function of the secretory and buffer systems of the stomach that control the relative acidity or alkalinity, as measured by the concentration of the hydrogen ion" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Brca2tm1Brn/Brca2tm1Brn,Trp53bp1tm1Jc/Trp53bp1tm1Jc,Cd19tm1(cre)Cgn/Cd19+ Genetic Background: involves: 129P2/OlaHsd
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MP:0008056 | abnormal retinal ganglion cell morphology | "any structural anomaly of ganglion neurons located in the innermost nuclear layer of the retina of that receive visual information from photoreceptors via various intermediate cells such as bipolar cells, amacrine cells, and horizontal cells; axons from these cells form the optic nerve and connect mainly to the lateral geniculate nucleus (LGN) and to the suprachiasmatic nucleus in the brain" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Shhtm1Amc/Shhtm2Amc,Tg(Thy1-cre)703Vaw/? Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C3H * C57BL/6
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MP:0008291 | abnormal adrenocortical cell morphology | "any structural anomaly of the steroid hormone-producing cells of the cortex of the adrenal gland" [MGI:llw2 "Linda Washburn, Mouse Genome Informatics Curator"] |
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Allelic Composition: Edardl-J/Edardl-J Genetic Background: involves: C3HeB/FeJ
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MP:0008302 | thin adrenal cortex | "reduced thickness of the thick outer layer of the adrenal gland that produces and secretes steroid hormones such as corticosterone, estrone and aldosterone" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Edardl-J/Edardl-J Genetic Background: involves: C3HeB/FeJ
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MP:0008489 | postnatal slow weight gain | "the weight gain over a span of postnatal developmental time is slower than controls, with or without ever attaining a similar weight to controls as adults" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Map1stm1.1Lliu/Map1stm1.1Lliu,Tg(CAG-EGFP/Map1lc3b)53Nmz/0 Genetic Background: involves: 129S4/SvJaeSor * C57BL/6 * C57BL/6NCrj
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MP:0008540 | abnormal cerebrum morphology | "any structural anomaly of the largest part of the brain, derived from the telencephalon, and is composed of a right and a left hemisphere each which contains an outer cerebral cortex and a subcortical basal ganglia; cerebral functions include sensorimotor, emotional, and intellectual activities" [MESH:A08.186.211.730.885.287] |
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Allelic Composition: Six3tm3.1Gco/Six3+,Shhtm1Chg/Shh+ Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
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MP:0008947 | increased neuron number | "greater than normal numbers of the cells of the nervous system that receive, conduct, and transmit impulses" [MESH:A08.663] |
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Allelic Composition: Shhtm1Ahk/Shhtm1Ahk,Slc6a3tm1(cre)Xz/Slc6a3+ Genetic Background: involves: 129S1/Sv * C57BL/6
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MP:0008948 | decreased neuron number | "fewer than normal numbers of the cells of the nervous system that receive, conduct, and transmit impulses" [MESH:A08.663] |
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Allelic Composition: Shhtm1Ahk/Shhtm1Ahk,Slc6a3tm1(cre)Xz/Slc6a3+ Genetic Background: involves: 129S1/Sv * C57BL/6
Allelic Composition: Wnt1tm1.1Mze/Wnt1tm1.1Mze,Gt(ROSA)26Sortm14(CAG-tdTomato)Hze/Gt(ROSA)26Sor+,Shhtm1(EGFP/cre)Cjt/Shh+ Genetic Background: involves: 129S6/SvEvTac * C57BL/6N
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MP:0008985 | hemimelia | "congenital absence of part of an extremity, such as absent fibula with the tibia present" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"] |
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Allelic Composition: ShhDz/ShhDz Genetic Background: C57BL/6J-ShhDz
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MP:0009204 | absent external male genitalia | "absence of the external masculine genital organs, including the penis and scrotum" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: ShhDsh/ShhDsh Genetic Background: involves: 101 * C3H * C57BL * SEC
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MP:0009211 | absent external female genitalia | "absence of the external feminine genital organs, collectively known as the vulva" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"] |
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Allelic Composition: ShhDsh/ShhDsh Genetic Background: involves: 101 * C3H * C57BL * SEC
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MP:0009493 | abnormal cystic duct morphology | "any structural anomaly of the tubular structure that conducts gall bladder contents from the gall bladder to the common bile duct" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"] |
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Allelic Composition: Lamp1tm1Psa/Lamp1tm1Psa,Lamp2tm1Psa/Y Genetic Background: involves: 129P2/OlaHsd * C57BL/6
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MP:0009545 | abnormal dermis papillary layer | "any structural anomaly of the more superficial, thin layer of the dermis that interdigitates with the epidermis" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"] |
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Allelic Composition: Shhtm1Amc/Shhtm1Amc Genetic Background: involves: 129/Sv * C57BL/6J * CBA/J
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MP:0009579 | acephaly | "congenital absence of the head" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"] |
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Allelic Composition: Lamp1tm1Psa/Lamp1tm1Psa,Lamp2tm1Psa/Y Genetic Background: involves: 129P2/OlaHsd * C57BL/6
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MP:0009584 | decreased keratinocyte proliferation | "reduction in the expansion rate of keratinocytes by cell division" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"] |
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Allelic Composition: Shhtm1Amc/Shhtm1Amc Genetic Background: involves: 129/Sv * C57BL/6J * CBA/J
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MP:0009703 | decreased birth body size | "reduction in average body size at birth compared to controls" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"] |
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Allelic Composition: Pofut1tm2Pst/Pofut1tm1Pst,Shhtm2(cre/ERT2)Cjt/Shh+ Genetic Background: involves: 129/Sv * 129S6/SvEvTac * C57BL/6J * SJL
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MP:0009743 | preaxial polydactyly | "duplication of all or part of the first ray on one or more of the autopods" [PMID:19125433] |
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Allelic Composition: Disp1tm1Pab/Disp1tm1Pab,Shhtm2Chg/Shh+,Edil3Tg(Sox2-cre)1Amc/Edil3+ Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA
Allelic Composition: Gt(ROSA)26Sortm1(Grem1)Svok/Gt(ROSA)26Sor+,Shhtm1(EGFP/cre)Cjt/0 Genetic Background: involves: 129S1/Sv
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MP:0009744 | postaxial polydactyly | "duplication of all or part of any of the rays except the first ray on one or more of the autopods" [PMID:19125433] |
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Allelic Composition: Gt(ROSA)26Sortm1(Grem1)Svok/Gt(ROSA)26Sor+,Shhtm1(EGFP/cre)Cjt/0 Genetic Background: involves: 129S1/Sv
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MP:0009844 | abnormal neural crest cell apoptosis | "change in the timing or the number of neural crest cells undergoing programmed cell death" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Shhtm1Chg/Shhtm2Amc,Nkx2-5tm1(cre)Rjs/Nkx2-5+ Genetic Background: involves: 129S1/Sv * 129S7/SvEvBrd * 129X1/SvJ
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MP:0009883 | palatal shelf hypoplasia | "reduced size of the palatal projections from the inner part of the maxillary processes that fuse to form the secondary palate, often due to reduced cell number" [PMID:16680722] |
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Allelic Composition: Shhtm1Amc/Shhtm2Amc,Tg(KRT14-cre)1Amc/0 Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA
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MP:0009887 | abnormal palatal shelf fusion at midline | "any anomaly in the process in which the palatal shelves grow toward the midline and adhere along the medial edge epithelia, forming the midline epithelial seam which disappears in later stages" [PMID:16942766] |
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Allelic Composition: Shhtm1Amc/Shhtm2Amc,Tg(KRT14-cre)1Amc/0 Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA
Allelic Composition: Six3tm3.1Gco/Six3+,Shhtm1Chg/Shh+ Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
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MP:0009888 | palatal shelves fail to meet at midline | "polarized growth towards the midline following palatal shelf elevation does not occur" [PMID:16942766] |
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Allelic Composition: Shhtm2Chg/Shh+,Edil3Tg(Sox2-cre)1Amc/Edil3+ Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA
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MP:0009890 | cleft secondary palate | "congenital fissure of the tissues normally uniting to form the secondary palate" [PMID:16680722] |
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Allelic Composition: Shhtm1Amc/Shhtm2Amc,Tg(KRT14-cre)1Amc/0 Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA
Allelic Composition: Shhtm2Chg/Shh+,Edil3Tg(Sox2-cre)1Amc/Edil3+ Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA
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MP:0009901 | abnormal frontonasal prominence morphology | "any structural anomaly of an unpaired facial process in the embryo formed from the tissues surrounding the forebrain vesicle that develops into the forehead and bridge of the nose/snout" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"] |
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Allelic Composition: Disp1icb/Disp1icb Genetic Background: involves: 129/Sv * C57BL/6J * SWR
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MP:0009903 | abnormal medial nasal prominence morphology | "any structural anomaly of the central area of the two limbs of a horseshoe-shaped mesenchymal swelling that lie medial to the olfactory placode or pit in the future nasal region of the embryo; it joins with the ipsilateral maxillary prominence in the formation of half of the upper jaw, and the nasal tip and philtrum of the upper lip develop from it" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"] |
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Allelic Composition: Six3tm3.1Gco/Six3+,Shhtm1Chg/Shh+ Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
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MP:0009905 | absent tongue | "absence of the mobile mass of muscular tissue and surrounding epithelial tissue occupying the cavity of the mouth and forming part of the floor" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"] |
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Allelic Composition: Ndst1tm1.1Grob/Ndst1+,Shhtm1Chg/Shh+ Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
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MP:0009937 | abnormal neuron differentiation | "abnormal growth or development of the cells of the nervous system that receive, conduct, and transmit impulses" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Disp1tm2.1Amc/Disp1tm2Amc,Shhtm1(EGFP/cre)Cjt/Shh+ Genetic Background: involves: 129/Sv * C57BL/6J * SWR
Allelic Composition: Disp1icb/Disp1tm2Amc,Shhtm1(EGFP/cre)Cjt/Shh+ Genetic Background: involves: 129/Sv * C57BL/6J * SWR
Allelic Composition: Disp1tm2.1Amc/Disp1tm2.1Amc,Shhtm1Amc/Shh+ Genetic Background: involves: 129/Sv * C57BL/6J * SWR
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MP:0010030 | abnormal orbit morphology | "any structural anomaly of the bony ring that supports the eyeball and supporting tissues and is formed by parts of several cranial bones" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"] |
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Allelic Composition: Ccd/Ccd+,ShhDsh/Shh+ Genetic Background: involves: 101 * C3H * C57BL * C57BL/10Rl * SEC
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MP:0010059 | olfactory bulb hypoplasia | "underdevelopment or reduced size, usually due to a reduced number of cells, of the forebrain region that coordinates neuronal signaling involved in the perception of smell" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition", MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Six3tm3.1Gco/Six3+,Shhtm1Chg/Shh+ Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
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MP:0010124 | decreased bone mineral content | "reduction in the amount (usually in grams/cm) of bone mineral divided by a bone-scanned area" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Setxtm1b(EUCOMM)Wtsi/Setxtm1b(EUCOMM)Wtsi Genetic Background: C57BL/6N-Setxtm1b(EUCOMM)Wtsi/Ics
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MP:0010149 | abnormal synaptic dopamine release | "aberrant secretion across synapses of the catecholamine neurotransmitter and neurohormone, derived from tyrosine and the precursor to norepinephrine and epinephrine; functions as a neurotransmitter in the brain and as a hormone to inhibit the release of prolactin from the anterior lobe of the pituitary" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Shhtm1Ahk/Shhtm1Ahk,Slc6a3tm1(cre)Xz/Slc6a3+ Genetic Background: involves: 129S1/Sv * C57BL/6
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MP:0010371 | abnormal epiglottis morphology | "any structural anomaly of the most superior of the laryngeal cartilages, which is found at the root of the tongue and folds back over the entrance to the larynx during swallowing, preventing inhalation of food or drink" [MGI:llw2 "Linda Washburn, Mouse Genome Informatics Curator"] |
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Allelic Composition: Ncr1m1J/Ncr1m1J,Pepcb/Pepcb,Ptprca/Ptprca Genetic Background: B6.SJL-Ptprca Pepcb/BoyJ
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MP:0010493 | abnormal atrium myocardium morphology | "any structural anomaly of the atrial part of middle layer of the heart, comprised of involuntary muscle" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"] |
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Allelic Composition: Lamp1tm1Psa/Lamp1tm1Psa,Lamp2tm1Psa/Y Genetic Background: involves: 129P2/OlaHsd * C57BL/6
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MP:0010646 | absent pulmonary vein | "absence of the veins that return oxygenated blood from the lungs to the left atrium of the heart" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Lamp1tm1Psa/Lamp1tm1Psa,Lamp2tm1Psa/Y Genetic Background: involves: 129P2/OlaHsd * C57BL/6
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MP:0010701 | fusion of atlas and odontoid process | "the large protuberance that projects upward from the cervical axis (C2), around which the cervical atlas normally rotates, is instead fused to elements of the atlas; the odontoid process may or may not remain attached to the axis" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: ShhDsh/Shh+ Genetic Background: B10Rl.Cg-ShhDsh
Allelic Composition: Ccd/Ccd+,ShhDsh/Shh+ Genetic Background: involves: 101 * C3H * C57BL * C57BL/10Rl * SEC
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MP:0010784 | abnormal forestomach morphology | "any structural anomaly of the dilated area of tissue where the stomach and esophagus meet" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Gt(ROSA)26Sortm1(CAG-Bmpr1a)Que/Gt(ROSA)26Sor+,Shhtm1(EGFP/cre)Cjt/? Genetic Background: Not Specified
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MP:0010825 | abnormal lung saccule morphology | "any structural anomaly of the transient dilations of the developing alveolar (or transient) ducts, which transform into a transitory alveolar duct as soon as it develops further branches; the last transitory saccule formed on each pathway is a terminal saccule that develops into an alveolar sac after birth" [GO:0060430, ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition", MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Shhtm1Amc/Shhtm1Amc Genetic Background: involves: 129/Sv * C57BL/6J * CBA/J
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MP:0010862 | decreased respiratory mucosa goblet cell number | "reduced number of the cells of the respiratory epithelial lining that produce and secrete mucins" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"] |
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Allelic Composition: Yy1tm2.1Yshi/Yy1tm2.1Yshi,Shhtm1(EGFP/cre)Cjt/Shh+ Genetic Background: involves: 129S4/SvJae * C57BL/6
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MP:0010883 | trachea stenosis | "abnormal narrowing or constriction of the trachea" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"] |
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Allelic Composition: Yy1tm2.1Yshi/Yy1tm2.1Yshi,Shhtm1(EGFP/cre)Cjt/Shh+ Genetic Background: involves: 129S4/SvJae * C57BL/6
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MP:0010897 | abnormal bronchiole epithelium morphology | "any structural anomaly of the epithelial layer of the bronchioles" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Pofut1tm2Pst/Pofut1tm1Pst,Shhtm2(cre/ERT2)Cjt/Shh+ Genetic Background: involves: 129/Sv * 129S6/SvEvTac * C57BL/6J * SJL
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MP:0010907 | absent lung buds | "absence of the blunt end of the respiratory diverticulum which normally grows ventrally out of the proximal end of the foregut, then extends caudally and divides into two, forming the origins of the bronchial tree" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"] |
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Allelic Composition: Ctnnb1tm2Kem/Ctnnb1tm2Kem,Shhtm1(EGFP/cre)Cjt/Shh+ Genetic Background: involves: 129S1/Sv * 129X1/SvJ
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MP:0010915 | increased solitary pulmonary neuroendocrine cell number | "increased number of the specialized non-ciliated, round- to oval-shaped epithelial cells found as solitary cells in the nasal respiratory epithelium and the mucosa of the larynx, trachea and bronchi up to the terminal bronchioles; PNECs are the first cell type to differentiate during early fetal lung development, produce amine (e.g. serotonin, 5-HT) and peptides (e.g. bombesin, calcitonin) with growth factor-like properties, and appear to be involved in processes ranging from lung development and respiratory physiology to repair, disease and carcinogenesis" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"] |
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Allelic Composition: Pofut1tm2Pst/Pofut1tm1Pst,Shhtm2(cre/ERT2)Cjt/Shh+ Genetic Background: involves: 129/Sv * 129S6/SvEvTac * C57BL/6J * SJL
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MP:0010940 | abnormal maxillary prominence morphology | |
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Allelic Composition: Ndst1tm1.1Grob/Ndst1+,Shhtm1Chg/Shh+ Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Allelic Composition: Ndst1tm1.1Grob/Ndst1tm1.1Grob,Shhtm1Chg/Shh+ Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
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MP:0010942 | abnormal respiratory epithelium morphology | "any structural anomaly of the pseudostratified ciliated epithelium that lines much of the conducting portion of the airway, including part of the nasal cavity and larynx, the trachea, and bronchi" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition", MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"] |
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Allelic Composition: Pofut1tm2Pst/Pofut1tm1Pst,Shhtm2(cre/ERT2)Cjt/Shh+ Genetic Background: involves: 129/Sv * 129S6/SvEvTac * C57BL/6J * SJL
Allelic Composition: Rbpjtm1Hon/Rbpjtm1.1Hon,Shhtm2(cre/ERT2)Cjt/Shh+ Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac
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MP:0010949 | decreased Clara cell number | "reduced number of the rounded, club-shaped, nonciliated cells found between ciliated cells in bronchiolar epithelium" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"] |
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Allelic Composition: Tmem107schlei/Tmem107tm1Lex Genetic Background: involves: 129S5/SvEvBrd * C3HeB/FeJ * C57BL/6J * C57BL/6N
Allelic Composition: Yy1tm2.1Yshi/Yy1tm2.1Yshi,Shhtm1(EGFP/cre)Cjt/Shh+ Genetic Background: involves: 129S4/SvJae * C57BL/6
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MP:0010975 | abnormal lung lobe morphology | "any structural anomaly of any of the anatomically and functionally distinct subunits (lobes) comprising the left or right lung, where each lobe receives air from its own secondary bronchus and is separated from it neighbors by one or more fissures (walls of connective tissue)" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"] |
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Allelic Composition: Shhtm1Amc/Shhtm1Amc,Tg(SFTPC-rtTA)5Jaw/0,Tg(tetO-Shh)1Jaw/0 Genetic Background: involves: FVB/N
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MP:0010976 | small lung lobe | "reduced size of any of the anatomically and functionally distinct subunits (lobes) comprising the left or right lung, where each lobe receives air from its own secondary bronchus and is separated from it neighbors by one or more fissures (walls of connective tissue)" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"] |
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Allelic Composition: Dicer1tm1Bdh/Dicer1tm1Bdh,Shhtm1(EGFP/cre)Cjt/Shh+ Genetic Background: involves: 129
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MP:0010994 | aerophagia | "excessive swallowing of air or gas" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"] |
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Allelic Composition: Shhtm1Amc/Shhtm2Amc,Tg(KRT14-cre)1Amc/0 Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA
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MP:0011011 | impaired lung lobe morphogenesis | "failure to form any of the anatomically and functionally distinct subunits (lobes) comprising the left or right lung" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"] |
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Allelic Composition: Shhtm1Amc/Shhtm1Amc Genetic Background: involves: 129/Sv * C57BL/6J * CBA/J
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MP:0011024 | abnormal branching involved in lung morphogenesis | "anomaly in the process in which the branched structure of the respiratory airway tree is generated and organized" [MGI:csmith] |
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Allelic Composition: Ednratm1Ywa/Ednratm1Ywa Genetic Background: involves: 129S7/SvEvBrd
Allelic Composition: Shhtm2Amc/Shhtm2Amc,Tg(SFTPC-rtTA)5Jaw/0,Tg(tetO-cre)1Jaw/0 Genetic Background: involves: FVB/N
Allelic Composition: Shhtm1Amc/Shhtm2Amc,Tg(SFTPC-rtTA)5Jaw/0,Tg(tetO-cre)1Jaw/0 Genetic Background: involves: FVB/N
Allelic Composition: Sox9tm1Gsr/Sox9tm1Gsr,Shhtm1(EGFP/cre)Cjt/Shh+ Genetic Background: involves: 129P2/OlaHsd
Allelic Composition: Dicer1tm1Mmk/Dicer1tm1Mmk,Shhtm1(EGFP/cre)Cjt/Shh+ Genetic Background: involves: 129 * C57BL/6J
Allelic Composition: Yy1tm2.1Yshi/Yy1tm2.1Yshi,Shhtm1(EGFP/cre)Cjt/Shh+ Genetic Background: involves: 129S4/SvJae * C57BL/6
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MP:0011028 | impaired branching involved in bronchus morphogenesis | |
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Allelic Composition: Shhtm1Amc/Shhtm1Amc Genetic Background: involves: 129/Sv * C57BL/6J * CBA/J
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MP:0011050 | abnormal respiratory motile cilium morphology | "any structural anomaly of the multiple epithelial tiny, motile hair-like projections, which have a variable arrangement of axonemal microtubules, contains molecular motors, and beat with a characteristic whip-like pattern that promote transport of fluids and other cells across the epithelium of the respiratory tract" [GO:0031514, MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"] |
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Allelic Composition: Igf1rtm1Jcbr/Igf1rtm1Jcbr,Tg(Scgb1a1-cre)1Tauc/0 Genetic Background: involves: C57BL/6
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MP:0011071 | absent Clara cells | "absence of the rounded, club-shaped, nonciliated cells found between ciliated cells in the bronchiolar epithelium" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"] |
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Allelic Composition: Pofut1tm2Pst/Pofut1tm1Pst,Shhtm2(cre/ERT2)Cjt/Shh+ Genetic Background: involves: 129/Sv * 129S6/SvEvTac * C57BL/6J * SJL
Allelic Composition: Rbpjtm1Hon/Rbpjtm1.1Hon,Shhtm2(cre/ERT2)Cjt/Shh+ Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac
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MP:0011085 | complete postnatal lethality | "premature death anytime between the neonatal period and weaning age of all organisms of a given genotype in a population (Mus: P1 to approximately 3 weeks of age)" [MGI:csmith] |
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Allelic Composition: Shhtm2Amc/Shhtm2Amc,Tg(Nes-cre)1Kln/0 Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL
Allelic Composition: Sox9tm1Gsr/Sox9tm1Gsr,Shhtm1(EGFP/cre)Cjt/Shh+ Genetic Background: involves: 129P2/OlaHsd
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MP:0011086 | partial postnatal lethality | "the appearance of lower than Mendelian ratios of organisms of a given genotype due to death of some, but not all of the organisms anytime between the neonatal period and weaning age (Mus: P1 to approximately 3 weeks of age)" [MGI:csmith] |
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Allelic Composition: Map1stm1.1Lliu/Map1stm1.1Lliu,Tg(CAG-EGFP/Map1lc3b)53Nmz/0 Genetic Background: involves: 129S4/SvJaeSor * C57BL/6 * C57BL/6NCrj
Allelic Composition: Pofut1tm2Pst/Pofut1tm1Pst,Shhtm2(cre/ERT2)Cjt/Shh+ Genetic Background: involves: 129/Sv * 129S6/SvEvTac * C57BL/6J * SJL
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MP:0011087 | complete neonatal lethality | "death of all organisms of a given genotype in a population within the neonatal period after birth (Mus: P0)" [MGI:csmith] |
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Allelic Composition: Ednratm1Ywa/Ednratm1Ywa Genetic Background: involves: 129S7/SvEvBrd
Allelic Composition: Shhtm2Amc/Shhtm2Amc,Tg(SFTPC-rtTA)5Jaw/0,Tg(tetO-cre)1Jaw/0 Genetic Background: involves: FVB/N
Allelic Composition: Shhtm1Amc/Shhtm2Amc,Tg(SFTPC-rtTA)5Jaw/0,Tg(tetO-cre)1Jaw/0 Genetic Background: involves: FVB/N
Allelic Composition: Shhtm1Amc/Shhtm1Amc,Tg(SFTPC-rtTA)5Jaw/0,Tg(tetO-Shh)1Jaw/0 Genetic Background: involves: FVB/N
Allelic Composition: Shhtm1Ptch/Shhtm1Ptch Genetic Background: involves: 129P2/OlaHsd * FVB/N * various
Allelic Composition: ShhDsh/ShhDsh Genetic Background: involves: 101 * C3H * C57BL * SEC
Allelic Composition: Shhtm1Amc/Shhtm2Amc,Tg(KRT14-cre)1Amc/0 Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA
Allelic Composition: Shhtm2Chg/Shhtm2Chg Genetic Background: involves: 129S1/Sv * 129X1/SvJ
Allelic Composition: Shhtm1Amc/Shhtm2Amc,Tg(Thy1-cre)703Vaw/? Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C3H * C57BL/6
Allelic Composition: Foxp1tm1.1Pwt/Foxp1tm1.1Pwt,Foxp4tm2.1Eem/Foxp4tm2.1Eem,Shhtm1(EGFP/cre)Cjt/Shh+ Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Allelic Composition: Yy1tm2.1Yshi/Yy1tm2.1Yshi,Shhtm1(EGFP/cre)Cjt/Shh+ Genetic Background: involves: 129S4/SvJae * C57BL/6
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MP:0011089 | complete perinatal lethality | "death of all organisms of a given genotype in a population within the perinatal period (Mus: E18.5 through postnatal day 1)" [MGI:csmith] |
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Allelic Composition: Disp1icb/Disp1icb Genetic Background: involves: 129/Sv * C57BL/6J * SWR
Allelic Composition: Shhtm1Amc/Shhtm1Amc Genetic Background: involves: 129/Sv * C57BL/6J * CBA/J
Allelic Composition: Shhtm2Chg/Shh+,Edil3Tg(Sox2-cre)1Amc/Edil3+ Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA
Allelic Composition: Disp1tm1Pab/Disp1tm1Pab,Shhtm2Chg/Shh+,Edil3Tg(Sox2-cre)1Amc/Edil3+ Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA
Allelic Composition: Dicer1tm1Bdh/Dicer1tm1Bdh,Shhtm1(EGFP/cre)Cjt/Shh+ Genetic Background: involves: 129
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MP:0011090 | partial perinatal lethality | "the appearance of lower than Mendelian ratios of organisms of a given genotype due to death of some, but not all of the organisms within the perinatal period (Mus: E18.5 through postnatal day 1)" [MGI:csmith] |
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Allelic Composition: Fgfr2tm1.1Dsn/Fgfr2+ Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Allelic Composition: Sox9tm1Gsr/Sox9tm1Gsr,Shhtm1(EGFP/cre)Cjt/Shh+ Genetic Background: involves: 129P2/OlaHsd
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MP:0011098 | complete embryonic lethality during organogenesis | "death of all organisms of a given genotype in a population between embryo turning and the completion of organogenesis (Mus: E9 to less than E14)" [MGI:csmith] |
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Allelic Composition: Gas1tm2Fan/Gas1tm2Fan,Shhtm1Chg/Shhtm1Chg Genetic Background: involves: 129/Sv * 129S1/Sv * 129X1/SvJ * C57BL/6J
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MP:0011100 | complete preweaning lethality | "death of all organisms of a given genotype in a population between fertilization and weaning age (Mus: approximately 3-4 weeks of age)" [MGI:csmith] |
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Allelic Composition: Jag1Yo/Jag1Yo Genetic Background: C3HeB/FeJ-Jag1Yo
Allelic Composition: Gt(ROSA)26Sortm1(CAG-Bmpr1a)Que/Gt(ROSA)26Sor+,Shhtm1(EGFP/cre)Cjt/? Genetic Background: Not Specified
Allelic Composition: Shhtm1b(EUCOMM)Wtsi/Shhtm1b(EUCOMM)Wtsi Genetic Background: C57BL/6N-Shhtm1b(EUCOMM)Wtsi/H
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MP:0011101 | partial prenatal lethality | "the appearance of lower than Mendelian ratios of organisms of a given genotype due to death of some, but not all of the organisms between fertilization and birth (Mus: approximately E18.5)" [MGI:csmith] |
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Allelic Composition: ShhDsh/ShhDsh Genetic Background: B10Rl.Cg-ShhDsh
Allelic Composition: Shhtm1Amc/Shhtm1Amc Genetic Background: involves: 129/Sv * C57BL/6J * CBA/J
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MP:0011108 | partial embryonic lethality during organogenesis | "the appearance of lower than Mendelian ratios of organisms of a given genotype due to death of some, but not all of the organisms between embryo turning and the completion of organogenesis (Mus: E9 to less than E14)" [MGI:csmith] |
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Allelic Composition: ShhDsh/ShhDsh Genetic Background: involves: 101 * C3H * C57BL * SEC
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MP:0011109 | partial lethality throughout fetal growth and development | "the appearance of lower than Mendelian ratios of organisms of a given genotype due to death of some, but not all of the organisms between the completion of organogenesis and birth (Mus: E14 to approximately E18.5)" [MGI:csmith] |
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Allelic Composition: Pbx1tm1Mlc/Pbx1tm2.1Mlc Genetic Background: involves: 129S6/SvEvTac
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MP:0011113 | abnormal airway basal cell morphology | "any structural anomaly of a long-lived multipotent stem cell of the pseudostratified airway epithelium which is restricted to the tracheal epithelium in mice; airway BCs have been shown to be capable of self renewal, give rise to secretory (Clara) cells and ciliated cells, and play important roles both in epithelial homeostasis and in pathological airway remodeling" [MGI:anna, PMID:20699479] |
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Allelic Composition: Yy1tm2.1Yshi/Yy1tm2.1Yshi,Shhtm1(EGFP/cre)Cjt/Shh+ Genetic Background: involves: 129S4/SvJae * C57BL/6
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MP:0011142 | abnormal lung-associated mesenchyme development | "abnormality in the formation of the lung tissue comprised of multiple cell types (including connective tissue, endothelial cells, lymphatics, smooth muscle cells surrounding airways and blood vessels, myofibroblasts involved in septum formation, and cartilage-forming cells in the trachea), with most cells thought to be derived from the splanchnic mesenchyme, and other cells (endothelial, smooth muscle) believed to invade the lung as it expands; lung mesenchyme is a critical determinant of the shape and size of the developing lung, the extent and patterning of epithelial branching, and the formation of the pulmonary vasculature and interstitial mesenchymal components of the adult lung" [MGI:anna, PMID:18533146, PMID:20048339] |
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Allelic Composition: Dicer1tm1Mmk/Dicer1tm1Mmk,Shhtm1(EGFP/cre)Cjt/Shh+ Genetic Background: involves: 129 * C57BL/6J
Allelic Composition: Yy1tm2.1Yshi/Yy1tm2.1Yshi,Shhtm1(EGFP/cre)Cjt/Shh+ Genetic Background: involves: 129S4/SvJae * C57BL/6
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MP:0011147 | increased mesenchymal cell proliferation involved in lung development | "increase in the expansion rate of a lung mesenchymal cell population by cell division" [MGI:anna] |
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Allelic Composition: Dicer1tm1Mmk/Dicer1tm1Mmk,Shhtm1(EGFP/cre)Cjt/Shh+ Genetic Background: involves: 129 * C57BL/6J
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MP:0011333 | abnormal kidney inner medulla morphology | "any structural anomaly of the inner medullary region of the adult kidney containing collecting ducts and the long loops of Henle" [MGI:csmith, PMID:20614633] |
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Allelic Composition: Smn1tm5(Smn1/SMN2)Mrph/Smn1tm5(Smn1/SMN2)Mrph Genetic Background: FVB.129(B6)-Smn1tm5(Smn1/SMN2)Mrph/J
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MP:0011360 | kidney cortex hypoplasia | "underdevelopment or reduced size, usually due to a reduced number of cells, of the outer portion of the kidney, which contains the renal corpuscles, the renal tubules (except for parts of the loop of Henle which descend into the renal medulla), blood vessels and cortical collecting ducts" [MGI:anna] |
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Allelic Composition: Smn1tm5(Smn1/SMN2)Mrph/Smn1tm5(Smn1/SMN2)Mrph Genetic Background: FVB.129(B6)-Smn1tm5(Smn1/SMN2)Mrph/J
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MP:0011378 | abnormal kidney outer medulla inner stripe morphology | "any structural anomaly of the deep, centrally located portion of the renal outer medulla that is traversed by thin descending and thick ascending portions of the loops of Henle" [GO:0072057] |
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Allelic Composition: Smn1tm5(Smn1/SMN2)Mrph/Smn1tm5(Smn1/SMN2)Mrph Genetic Background: FVB.129(B6)-Smn1tm5(Smn1/SMN2)Mrph/J
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MP:0011380 | enlarged brain ventricle | "increased size of one or more of the four communicating cavities within the brain that are continuous with the central canal of the spinal cord" [MGI:smb] |
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Allelic Composition: Shhtm2Chg/Shh+,Edil3Tg(Sox2-cre)1Amc/Edil3+ Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA
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MP:0011415 | abnormal aldosterone level | "anomaly in the concentration of the hormone that is secreted by the adrenal cortex and regulates sodium conservation and potassium secretion in the distal renal tubule" [ISBN:0-683-40008-8] |
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Allelic Composition: Nr5a1tm1.1Hain/Nr5a1tm1.1Hain,Shhtm1Amc/Shh+ Genetic Background: involves: 129S1/Sv * 129X1/SvJ
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MP:0011426 | abnormal ureter smooth muscle morphology | "any structural anomaly of the smooth muscle tissue surrounding the epithelium of the ureter" [MGI:anna] |
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Allelic Composition: Smn1tm5(Smn1/SMN2)Mrph/Smn1tm5(Smn1/SMN2)Mrph Genetic Background: FVB.129(B6)-Smn1tm5(Smn1/SMN2)Mrph/J
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MP:0011485 | abnormal urethra urothelium morphology | "any structural anomaly of the epithelial lining of the luminal space of the urethra" [MGI:csmith] |
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Allelic Composition: Gt(ROSA)26Sortm2(Sp8)Lma/Gt(ROSA)26Sor+,Sp8tm1Smb/Sp8tm1Smb,Tg(Msx2-cre)5Rem/0 Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA
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MP:0011732 | decreased somite size | "reduced size of any of the segmental masses along the notochord of the developing embryo" [MGI:smb] |
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Allelic Composition: Fkbp8tm1Tili/Fkbp8tm1Tili,Shhtm1Chg/Shhtm1Chg Genetic Background: involves: C57BL/6
Allelic Composition: Shhtm1Chg/Shhtm1Chg Genetic Background: involves: C57BL/6
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MP:0011771 | abnormal genital tubercle morphology | "any structural anomaly of the embryonic anlage of the external genitalia, which emerges as paired swellings ventral to the cloacal membrane, is proposed to be derived from all three germ layers, and gives rise to the penis, clitoris, scrotum, labia, and foreskin; GT development is indistinguishable in male and female mouse embryos until approximately E16, when the urethral plate begins to be masculinized to form the penile urethra, marking the beginning of an androgen-dependent phase of sexual differentiation" [MGI:anna] |
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Allelic Composition: Il1r1tm1.1Rbl/Il1r1tm1.1Rbl Genetic Background: B6.129(Cg)-Il1r1tm1.1Rbl
Allelic Composition: Gt(ROSA)26Sortm1(Fgf8)Lma/Gt(ROSA)26Sor+,Shhtm2(cre/ERT2)Cjt/Shhtm2(cre/ERT2)Cjt Genetic Background: involves: 129S6/SvEvTac
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MP:0011805 | decreased cell migration | "reduced or slower movement of cells from one site to another, often occuring during developmental or chemotactic processes" [GO:0016477, MGI:csmith] |
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Allelic Composition: Sox9tm1Gsr/Sox9tm1Gsr,Shhtm1(EGFP/cre)Cjt/Shh+ Genetic Background: involves: 129P2/OlaHsd
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MP:0012089 | decreased midbrain size | "size reduction or truncation of the brain region derived from the middle of the three cerebral vesicles of the embryo; this region controls sensory and motor functions in the adult, including eye movement and coordination of auditory and visual reflexes" [MGI:anna, MGI:csmith] |
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Allelic Composition: Fgfr2tm1.1Dsn/Fgfr2+ Genetic Background: involves: 129P2/OlaHsd * C57BL/6
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MP:0012091 | increased midbrain size | "greater than average size of the brain region derived from the middle of the three cerebral vesicles of the embryo; this region controls sensory and motor functions in the adult, including eye movement and coordination of auditory and visual reflexes" [MGI:anna, MGI:csmith] |
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Allelic Composition: Shhtm2Chg/Shh+,Edil3Tg(Sox2-cre)1Amc/Edil3+ Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA
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MP:0012139 | increased forebrain size | "greater than average size of the anterior of the three primary divisions of the developing chordate brain or the corresponding part of the adult brain (in vertebrates, includes especially the cerebral hemispheres, the thalamus, and the hypothalamus and especially in higher vertebrates is the main control center for sensory and associative information processing, visceral functions, and voluntary motor functions)" [GO:0048853] |
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Allelic Composition: Shhtm2Chg/Shh+,Edil3Tg(Sox2-cre)1Amc/Edil3+ Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA
Allelic Composition: Tctn1Gt(KST296)Byg/Tctn1Gt(KST296)Byg,Shhtm1Chg/Shhtm1Chg Genetic Background: involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6
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MP:0012197 | impaired myofibroblast differentiation | |
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Allelic Composition: Yy1tm2.1Yshi/Yy1tm2.1Yshi,Shhtm1(EGFP/cre)Cjt/Shh+ Genetic Background: involves: 129S4/SvJae * C57BL/6
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MP:0012257 | absent philtrum | "absence of the vertical groove normally found on the median line of the upper lip" [MGI:anna] |
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Allelic Composition: Six3tm3.1Gco/Six3+,Shhtm1Chg/Shh+ Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
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MP:0012270 | cardiac edema | "abnormal accumulation of fluid in the interstitial tissues and cavities of the body due to impaired cardiac function or congestive heart failure; usually characterized by increased venous and capillary pressures and often associated with renal sodium retention" [MGI:anna] |
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Allelic Composition: Gas1tm2Fan/Gas1tm2Fan,Shhtm1Chg/Shhtm1Chg Genetic Background: involves: 129/Sv * 129S1/Sv * 129X1/SvJ * C57BL/6J
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MP:0012517 | absent diencephalon | "absence or loss of the paired caudal parts of the prosencephalon from which the thalamus, hypothalamus, epithalamus and subthalamus are derived; these regions regulate autonomic, visceral and endocrine function, and process information directed to the cerebral cortex" [MGI:anna] |
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Allelic Composition: Fgfr2tm1.1Dsn/Fgfr2+ Genetic Background: involves: 129P2/OlaHsd * C57BL/6
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MP:0013293 | embryonic lethality prior to tooth bud stage | "death prior to the appearance of tooth buds (Mus: E12-E12.5)" [MGI:smb] |
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Allelic Composition: Shhtm1b(EUCOMM)Wtsi/Shhtm1b(EUCOMM)Wtsi Genetic Background: C57BL/6N-Shhtm1b(EUCOMM)Wtsi/H
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MP:0013790 | single external naris | "presence of only one anterior opening to the nasal cavity as opposed to the normal two; usually associated with midline facial defects arising from cleavage anomalies" [MGI:Anna] |
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Allelic Composition: Gas1tm2Fan/Gas1tm2Fan,Shhtm1Chg/Shh+ Genetic Background: involves: 129/Sv * 129S1/Sv * 129X1/SvJ * C57BL/6J
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MP:0014101 | decreased chondrocyte proliferation | "decreased amount of multiplication or reproduction of chondrocytes by cell division, resulting in the expansion of their population" [GO:0035988] |
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Allelic Composition: ShhDsh/Shh+ Genetic Background: B10Rl.Cg-ShhDsh
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MP:0014105 | abnormal chondrocyte differentiation | "any anomaly in the process in which a chondroblast acquires specialized structural and/or functional features of a chondrocyte" [GO:0002062] |
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Allelic Composition: ShhDsh/Shh+ Genetic Background: B10Rl.Cg-ShhDsh
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MP:0014155 | absent olfactory epithelium | "absence of the epithelial cells that line the interior of the nose" [MGI:csmith] |
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Allelic Composition: Ndst1tm1.1Grob/Ndst1+,Shhtm1Chg/Shh+ Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
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MP:0014200 | abnormal respiratory epithelium physiology | "any functional anomaly of the pseudostratified ciliated epithelium that lines much of the conducting portion of the airway, including part of the nasal cavity and larynx, the trachea, and bronchi" [ISBN:0-683-40008-8, MGI:Anna] |
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Allelic Composition: Yy1tm2.1Yshi/Yy1tm2.1Yshi,Shhtm1(EGFP/cre)Cjt/Shh+ Genetic Background: involves: 129S4/SvJae * C57BL/6
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MP:0020134 | abnormal gallbladder size | "an anomaly in the size of the gall bladder compared to average, the organ that serves as a storage reservoir for bile" [GOC:NV] |
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Allelic Composition: Lamp1tm1Psa/Lamp1tm1Psa,Lamp2tm1Psa/Y Genetic Background: involves: 129P2/OlaHsd * C57BL/6
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MP:0020516 | abnormal visceral yolk sac mesenchyme morphology | "any structural anomaly of the portion of the visceral yolk sac that is derived from mesoderm and consists of mesenchyme" [UBERON:0003316] |
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Allelic Composition: Tyrc-32DSD/Tyrc Genetic Background: involves: 101/Rl * C3H/Rl
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MP:0020530 | disorganized thalamus | "derangement of the pattern of thalamic tissues" [MGI:smb] |
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Allelic Composition: Shhtm2Amc/Shhtm2Amc,Tg(Nes-cre)1Kln/0 Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL
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MP:0030002 | increased lung apoptosis | "acceleration in the timing or in the number of cells of the lung undergoing programmed cell death" [ORCID:orcid.org/0000-0002-6490-7723, PMID:17589521] |
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Allelic Composition: Yy1tm2.1Yshi/Yy1tm2.1Yshi,Shhtm1(EGFP/cre)Cjt/Shh+ Genetic Background: involves: 129S4/SvJae * C57BL/6
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MP:0030079 | small incisors | "reduced size of the set of long teeth that are the most anterior and prominent in the jaw" [MGI:anna] |
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Allelic Composition: Shhtm1Amc/Shhtm2Amc,Tg(KRT14-cre)1Amc/0 Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA
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MP:0030136 | abnormal lower incisor morphology | "any structural anomaly of the lower set of long teeth that are the most anterior and prominent in the jaw" [MGI:anna] |
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Allelic Composition: Shhtm1Amc/Shhtm2Amc,Tg(KRT14-cre)1Amc/0 Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA
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MP:0030190 | small snout | "decreased size of the anterior facial part of the face or muzzle containing the oral and nasal regions" [MGI:anna] |
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Allelic Composition: Ndst1tm1.1Grob/Ndst1+,Shhtm1Chg/Shh+ Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
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MP:0030250 | frontonasal prominence hypoplasia | "underdevelopment or reduced size, usually due to a reduced number of cells, of the unpaired embryonic process that is formed from the tissues surrounding the forebrain vesicle and develops into the forehead and bridge of the nose/snout" [MGI:anna] |
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Allelic Composition: Ndst1tm1.1Grob/Ndst1+,Shhtm1Chg/Shh+ Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Allelic Composition: Ndst1tm1.1Grob/Ndst1tm1.1Grob,Shhtm1Chg/Shh+ Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
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MP:0030277 | thin interparietal bone | "reduced thickness of the bone of the cranium that lies above and anterior to the occipital bone in some mammals" [MGI:anna] |
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Allelic Composition: ShhDsh/Shh+ Genetic Background: B10Rl.Cg-ShhDsh
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MP:0030453 | abnormal odontoblast morphology | "any structural anomaly of the skeletogenic cell on the outer surface of the dental pulp that secretes dentin matrix, is derived from the odontogenic papilla, and develops from a preodontoblast cell" [CL:0000060, GO:0071895] |
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Allelic Composition: Shhtm1Amc/Shhtm2Amc,Tg(KRT14-cre)1Amc/0 Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA
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MP:0030457 | abnormal molar cusp morphology | "any structural anomaly of an elevation or mound on the crown of a molar tooth making up a part of the occlusal (masticatory) surface" [https://medical-dictionary.thefreedictionary.com/cusp+of+tooth, MGI:anna] |
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Allelic Composition: Shhtm1Amc/Shhtm2Amc,Tg(KRT14-cre)1Amc/0 Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA
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MP:0030527 | absent enamel cord | "missing the transient structure of the dental (enamel) organ that is normally present at the early cap stage of molar tooth development; the enamel cord is a strand of epithelial cells that runs from (links) the enamel knot to the outer dental epithelial cells, dividing the dental organ into two parts" [https://en.wikipedia.org/wiki/Enamel_cord, ISBN:978-0-12-597951-1, MGI:anna] |
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Allelic Composition: Shhtm1Amc/Shhtm2Amc,Tg(KRT14-cre)1Amc/0 Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA
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