MP:0000035 | abnormal membranous labyrinth | "malformations in the complex arrangement of communicating canaliculi and sacs suspended within the cavity of the bony labyrinth of the inner ear" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, J:23837] |
Show
Allelic Composition: Fignfi/Fignfi Genetic Background: mixed
|
MP:0000036 | absent semicircular canals | "missing organ of balance; consists of three bony tubes within which the semicircular ducts are located" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:23837] |
Show
Allelic Composition: Fignfi/Fignfi Genetic Background: mixed
Allelic Composition: Figntm1Frk/Fignfi Genetic Background: involves: 129S1/Sv * 129X1SvJ * C57BL/6J
|
MP:0000458 | abnormal mandible morphology | "malformation 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] |
Show
Allelic Composition: Jag2tm1Grid/Jag2tm1Grid,Lfngtm1Grid/Lfng+ Genetic Background: involves: 129S1/Sv * C57BL/6J
|
MP:0000562 | polydactyly | "greater than 5 digits on one or more autopods" [Stedman s Medical Dictionary:ISBN 0-683-40008-8] |
Show
Allelic Composition: Jag2tm1Grid/Jag2tm1Grid,Lfngtm1Grid/Lfng+ Genetic Background: involves: 129S1/Sv * C57BL/6J
|
MP:0000929 | open neural tube | "incomplete invagination and fusion of the neuroepithelial layer in early development" [MGI:CLS, J:53370, J:62571] |
Show
Allelic Composition: Fignfi/Fignfi,Pax3Sp/Pax3Sp Genetic Background: BR.Cg-Pax3Sp Fignfi
|
MP:0001262 | decreased body weight | "lower than normal average weight " [J:61295] |
Show
Allelic Composition: Jag2tm1Grid/Jag2tm1Grid,Lfngtm1Grid/Lfng+ Genetic Background: involves: 129S1/Sv * C57BL/6J
|
MP:0001297 | microphthalmia | "reduced average size of the eyes" [J:18048] |
Show
Allelic Composition: Prkdcscid/Prkdcscid,Iduatm1Clk/Iduatm1Clk Genetic Background: NOD.129(B6)-Prkdcscid Iduatm1Clk/J
Allelic Composition: Fignfi/Fignfi Genetic Background: mixed
Allelic Composition: Figntm1Frk/Fignfi Genetic Background: involves: 129S1/Sv * 129X1SvJ * C57BL/6J
|
MP:0001306 | small lens | "reduced size of the transparent structure of the eye responsible for focusing light rays" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:49840] |
Show
Allelic Composition: Jag2tm1Grid/Jag2tm1Grid,Lfngtm1Grid/Lfng+ Genetic Background: involves: 129S1/Sv * C57BL/6J
|
MP:0001312 | abnormal cornea morphology | "malformation or absence of the transparent anterior portion of the fibrous coat of the eye that serves as the chief refractory structure " [MeSH:National Library of Medicine - Medical Subject Headings , 2003, Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8] |
Show
Allelic Composition: Jag2tm1Grid/Jag2tm1Grid,Lfngtm1Grid/Lfng+ Genetic Background: involves: 129S1/Sv * C57BL/6J
|
MP:0001314 | corneal opacity | "complete or partial clouding of the cornea" [jte:Janan T. Eppig , Mouse Genome Informatics, Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8] |
Show
Allelic Composition: Jag2tm1Grid/Jag2tm1Grid,Lfngtm1Grid/Lfng+ Genetic Background: involves: 129S1/Sv * C57BL/6J
|
MP:0001347 | absent lacrimal glands | "missing the glands that secrete tears" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, tc:Teresa Chu , Mouse Genome Informatics Curator] |
Show
Allelic Composition: Jag2tm1Grid/Jag2tm1Grid,Lfngtm1Grid/Lfng+ Genetic Background: involves: 129S1/Sv * C57BL/6J
|
MP:0001386 | abnormal maternal nurturing | "failure of mothers to tend offspring" [J:39801] |
Show
Allelic Composition: Jag2tm1Grid/Jag2tm1Grid,Lfngtm1Grid/Lfng+ Genetic Background: involves: 129S1/Sv * C57BL/6J
|
MP:0001395 | bi-directional circling | "circling behavior exhibited in both clockwise and counterclockwise directions" [cml:Cathleen M. Lutz , Mouse Genome Informatics Curator] |
Show
Allelic Composition: Fignfi/Fignfi Genetic Background: mixed
|
MP:0001405 | impaired coordination | "reduced ability to execute integrated movements of muscle" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator, Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8] |
Show
Allelic Composition: Jag2tm1Grid/Jag2tm1Grid,Lfngtm1Grid/Lfng+ Genetic Background: involves: 129S1/Sv * C57BL/6J
|
MP:0001488 | increased startle reflex | "reduced threshold or more severe reflex response to variable stimuli, often auditory; usually measured by amplitude of whole body flinch" [What s Wrong With My Mouse?:ISBN 0-471-31639-3, csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
Show
Allelic Composition: Jag2tm1Grid/Jag2tm1Grid,Lfngtm1Grid/Lfng+ Genetic Background: involves: 129S1/Sv * C57BL/6J
|
MP:0001575 | cyanosis | "a dark bluish or purple skin discoloration resulting from deficient oxygenation of the blood" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:60159] |
Show
Allelic Composition: Gata3tm2Gsv/Gata3+ Genetic Background: either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129S7/SvEvBrd * C57BL/6)
|
MP:0001732 | postnatal growth retardation | "slow or limited development after birth " [Stedman s Medical Dictionary:ISBN 0-683-40008-8] |
Show
Allelic Composition: Fignfi/Fignfi Genetic Background: mixed
|
MP:0001851 | eye inflammation | "local accumulation of fluid, plasma proteins, and leukocytes in the eye" [Immunobiology , The Immune System in Health and Disease:ISBN 0-8153-1691-7, cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator] |
Show
Allelic Composition: Fignfi/Fignfi Genetic Background: mixed
|
MP:0001852 | conjunctivitis | "inflammation of the mucous membrane that lines the inner surface of the eyelids" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:60896] |
Show
Allelic Composition: Fignfi/Fignfi Genetic Background: mixed
|
MP:0001921 | reduced fertility | "diminished ability to produce live offspring" [J:65030] |
Show
Allelic Composition: Jag2tm1Grid/Jag2tm1Grid,Lfngtm1Grid/Lfng+ Genetic Background: involves: 129S1/Sv * C57BL/6J
|
MP:0001954 | respiratory distress | "physical difficulty or inability to breathe" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:54931] |
Show
Allelic Composition: Gata3tm2Gsv/Gata3+ Genetic Background: either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129S7/SvEvBrd * C57BL/6)
|
MP:0001967 | deafness | "inability to hear" [J:57651] |
Show
Allelic Composition: Fignfi/Fignfi Genetic Background: mixed
|
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] |
Show
Allelic Composition: Jag2tm1Grid/Jag2tm1Grid,Lfngtm1Grid/Lfng+ Genetic Background: involves: 129S1/Sv * C57BL/6J
|
MP:0002428 | abnormal semicircular canal | "anomaly of the organ of balance composed of three long bony tubes of the labyrinth" [MeSH:National Library of Medicine - Medical Subject Headings , 2003, cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator] |
Show
Allelic Composition: Figntm1Frk/Fignfi Genetic Background: involves: 129S1/Sv * 129X1SvJ * C57BL/6J
|
MP:0002730 | head shaking | "compulsive movement of the head in the horizontal plane" [pvb:Pierre Vanden Borre , Mouse Genome Informatics Curator, J:274] |
Show
Allelic Composition: Prkdcscid/Prkdcscid,Iduatm1Clk/Iduatm1Clk Genetic Background: NOD.129(B6)-Prkdcscid Iduatm1Clk/J
Allelic Composition: Fignfi/Fignfi Genetic Background: mixed
Allelic Composition: Figntm1Frk/Fignfi Genetic Background: involves: 129S1/Sv * 129X1SvJ * C57BL/6J
|
MP:0003077 | abnormal cell cycle | "failure to progress or abnormal progression through the stages of of the cell cycle" [smb:Susan M. Bello, Mouse Genome Informatics Curator, J:91266] |
Show
Allelic Composition: Fignfi/Fignfi Genetic Background: mixed
|
MP:0003161 | absent lateral semicircular canal | |
Show
Allelic Composition: Fignfi/Fignfi Genetic Background: mixed
|
MP:0003312 | abnormal locomotor coordination | "reduced ability of an animal to maintain skillful and effective interaction of movements while engaging in locomotor activity" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
Show
Allelic Composition: Fignfi/Fignfi Genetic Background: mixed
|
MP:0004045 | abnormal cell cycle checkpoint function | "anomaly in the amount of time spent at the points in the cell cycle (end of G1 phase, end of G2 phase, and during metaphase) which prevent the cell from progressing to the next phase when conditions are unfavorable" [smb:Susan M Bello, Mouse Genome Informatics Curator] |
Show
Allelic Composition: Gt(ROSA)26Sortm1(GRN)Pvd/Gt(ROSA)26Sortm1(GRN)Pvd,Tg(Pgk1-cre)1Lni/0,Tg(SOD1*G93A)1Gur/0 Genetic Background: B6J.Cg-Tg(Pgk1-cre)1Lni Gt(ROSA)26Sortm1(GRN)Pvd Tg(SOD1*G93A)1Gur
|
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"] |
Show
Allelic Composition: Fignfi/Fignfi Genetic Background: mixed
|
MP:0004748 | increased susceptibility to age-related hearing loss | "greater than normal loss of hearing associated with advancing age, manifest as reduced ability to perceive or discriminate sounds; the pattern and age of onset vary" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"] |
Show
Allelic Composition: Fignfi/Fignfi Genetic Background: mixed
|
MP:0005542 | corneal vascularization | "formation of blood vessels in the cornea, which normally lacks vessels" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator, Stedman s Medical Dictionary:ISBN 0-683-40008-8] |
Show
Allelic Composition: Fignfi/Fignfi Genetic Background: mixed
|
MP:0006071 | abnormal retinal progenitor morphology | "anomoly in the proliferation or differentiation of the cells that give rise to the various cells of the retina" [smb:Susan M Bello, Mouse Genome Informatics Curator, J:92622:] |
Show
Allelic Composition: Fignfi/Fignfi Genetic Background: mixed
|
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] |
Show
Allelic Composition: Fignfi/Fignfi Genetic Background: mixed
|
MP:0008919 | fused tarsal bones | "anomaly of the eight bones of the instep of the paw/foot resulting in some or all the bones being joined together" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"] |
Show
Allelic Composition: Fignfi/Fignfi Genetic Background: mixed
|
MP:0009772 | abnormal retinal development | "anomaly in any of the steps during embryogenesis that produce the nerve layer lining in the back of the eye which senses light, and creates impulses that travel through the optic nerve to the brain" [MGI:llw2 "Linda Washburn, Mouse Genome Informatics Curator"] |
Show
Allelic Composition: Fignfi/Fignfi Genetic Background: mixed
|
MP:0009890 | cleft secondary palate | "congenital fissure of the tissues normally uniting to form the secondary palate" [PMID:16680722] |
Show
Allelic Composition: Gata3tm2Gsv/Gata3+ Genetic Background: either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129S7/SvEvBrd * C57BL/6)
Allelic Composition: Akap8Gt(XG068)Byg/Akap8+,Fignfi/Fignfi Genetic Background: involves: 129P2/OlaHsd * 129S1/SvImJ * C57BL/6
Allelic Composition: Akap8Gt(XG068)Byg/Akap8Gt(XG068)Byg,Fignfi/Fign+ Genetic Background: involves: 129P2/OlaHsd * 129S1/SvImJ * C57BL/6
Allelic Composition: Fignfi/Fignfi Genetic Background: involves: 129P2/OlaHsd * 129S1/SvImJ * C57BL/6
Allelic Composition: Fignfi/Fignfi Genetic Background: involves: 129S1/SvImJ * C57BL/6
|
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] |
Show
Allelic Composition: Gata3tm2Gsv/Gata3+ Genetic Background: either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129S7/SvEvBrd * C57BL/6)
|
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] |
Show
Allelic Composition: Prkdcscid/Prkdcscid,Iduatm1Clk/Iduatm1Clk Genetic Background: NOD.129(B6)-Prkdcscid Iduatm1Clk/J
|
MP:0011088 | partial neonatal 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 neonatal period after birth (Mus: P0)" [MGI:csmith] |
Show
Allelic Composition: Gata3tm2Gsv/Gata3+ Genetic Background: either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129S7/SvEvBrd * C57BL/6)
|
MP:0011091 | complete prenatal lethality | "death of all organisms of a given genotype in a population between fertilization and birth (Mus: approximately E18.5)" [MGI:csmith] |
Show
Allelic Composition: Fignfi/Fignfi,Pax3Sp/Pax3Sp Genetic Background: BR.Cg-Pax3Sp Fignfi
|
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] |
Show
Allelic Composition: Prkdcscid/Prkdcscid,Iduatm1Clk/Iduatm1Clk Genetic Background: NOD.129(B6)-Prkdcscid Iduatm1Clk/J
|
MP:0013387 | Meibomian gland hypertrophy | "increase in the bulk size of the meibum-secreting modified lobulated sebaceous glands located at the rim of the eyelids inside the tarsal plate due to cell enlargement" [MGI:Anna] |
Show
Allelic Composition: Fignfi/Fignfi Genetic Background: mixed
|
MP:0013447 | Harderian gland hypertrophy | "increase in the bulk size, due to cell enlargement, of the sebaceous gland that is located behind the eyeball and excretes fluid that facilitates movement of the nictitating membrane" [MGI:Anna] |
Show
Allelic Composition: Fignfi/Fignfi Genetic Background: mixed
|
MP:0030233 | absent mandibular canal | "absence of the canal that is normally located within the internal aspect of the mandible and contains the inferior alveolar nerve, artery and the vein" [MGI:anna] |
Show
Allelic Composition: Fignfi/Fignfi Genetic Background: mixed
|
MP:0030235 | absent mandibular foramen | "absence of the opening that is normally located on the medial surface of the ramus of the mandible and forms the entrance to the mandibular canal" [MGI:anna] |
Show
Allelic Composition: Fignfi/Fignfi Genetic Background: mixed
|
MP:0030237 | absent mental foramen | "absence of the small opening located on the anterior surface of the mandible; normally, the mental nerve, a terminal branch of inferior alveolar nerve, and the mental artery leave the mandibular canal through it" [MGI:anna] |
Show
Allelic Composition: Fignfi/Fignfi Genetic Background: mixed
|