MP:0000108 | midline facial cleft | "incomplete merging or fusion of the tissues normally uniting to form the face" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:49840] |
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Allelic Composition: Spta1sph-3J/Spta1sph-3J Genetic Background: NOD.Cg-H2b Spta1sph-3J
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MP:0000267 | abnormal cardiac development | "aberrant formation or incomplete differentiation of the heart" [MGI:cls, J:53370] |
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Allelic Composition: Rdh10tm1.1Ics/Rdh10tm1.1Ics Genetic Background: involves: C57BL/6 * SJL
Allelic Composition: Rdh10tm2Ics/Rdh10tm2Ics Genetic Background: Not Specified
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MP:0000269 | abnormal looping morphogenesis | "atypical bending of the primitive heart tube during early development" [J:27443] |
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Allelic Composition: Aldh1a2grim/Aldh1a2grim Genetic Background: involves: 129S1/Sv * C57BL/6
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MP:0000270 | abnormal heart tube morphology | "malformed embryonic heart " [J:37888] |
Show
Allelic Composition: Rdh10tm1.1Ics/Rdh10tm1.1Ics Genetic Background: involves: C57BL/6 * SJL
Allelic Composition: Rdh10tm2Ics/Rdh10tm2Ics Genetic Background: Not Specified
Allelic Composition: Rdh10tm1a(KOMP)Wtsi/Rdh10tm1a(KOMP)Wtsi Genetic Background: involves: C57BL/6J * C57BL/6N
Allelic Composition: Rdh10tm1d(KOMP)Wtsi/Rdh10tm1d(KOMP)Wtsi Genetic Background: involves: 129S4/SvJaeSor * C57BL/6J * C57BL/6N
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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] |
Show
Allelic Composition: Spta1sph-3J/Spta1sph-3J Genetic Background: NOD.Cg-H2b Spta1sph-3J
Allelic Composition: Rdh10m366Asp/Rdh10m366Asp Genetic Background: involves: C57BL/6J
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MP:0000470 | abnormal stomach morphology | "malformation of the sac-like structure of the digestive canal between the esophagus and the small intestine" [Stedman s Medical Dictionary:ISBN 0-683-40008-8] |
Show
Allelic Composition: Rdh10tm1.1Ics/Rdh10tm1.1Ics Genetic Background: involves: C57BL/6 * SJL
Allelic Composition: Rdh10tm2Ics/Rdh10tm2Ics Genetic Background: Not Specified
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MP:0000477 | abnormal intestine morphology | "malformation of the digestive tube passing from the stomach to the anus" [J:48968] |
Show
Allelic Composition: Rdh10tm1.1Ics/Rdh10tm1.1Ics Genetic Background: involves: C57BL/6 * SJL
Allelic Composition: Rdh10tm2Ics/Rdh10tm2Ics Genetic Background: Not Specified
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MP:0000550 | abnormal forelimb morphology | "malformation of the entire anterior extremities" [MGI:tc] |
Show
Allelic Composition: Spta1sph-3J/Spta1sph-3J Genetic Background: NOD.Cg-H2b Spta1sph-3J
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MP:0000553 | absent radius | "missing the short bone of the lateral forearm" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:54637] |
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Allelic Composition: Spta1sph-3J/Spta1sph-3J Genetic Background: NOD.Cg-H2b Spta1sph-3J
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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] |
Show
Allelic Composition: Rdh10tm1.1Ics/Rdh10tm1.1Ics Genetic Background: involves: C57BL/6 * SJL
Allelic Composition: Rdh10tm2Ics/Rdh10tm2Ics Genetic Background: Not Specified
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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: Spta1sph-3J/Spta1sph-3J Genetic Background: NOD.Cg-H2b Spta1sph-3J
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MP:0000600 | liver hypoplasia | "reduced size of liver due to decreased cell number " [J:57631] |
Show
Allelic Composition: Rdh10tm1.1Ics/Rdh10tm1.1Ics Genetic Background: involves: C57BL/6 * SJL
Allelic Composition: Rdh10tm2Ics/Rdh10tm2Ics Genetic Background: Not Specified
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MP:0000601 | small liver | "reduced size of the liver" [J:23170] |
Show
Allelic Composition: Spta1sph-3J/Spta1sph-3J Genetic Background: NOD.Cg-H2b Spta1sph-3J
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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] |
Show
Allelic Composition: Rdh10m366Asp/Rdh10m366Asp Genetic Background: involves: C57BL/6J
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MP:0000788 | abnormal cerebral cortex morphology | "malformed gray cellular mantle covering the surface of the brain" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, J:38857] |
Show
Allelic Composition: Rdh10m366Asp/Rdh10m366Asp Genetic Background: involves: C57BL/6J
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MP:0001081 | abnormal cranial ganglia morphology | "any anomaly, deformity, or malformation of the groups of nerve cell bodies associated with the twelve cranial nerves" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, MGI:cls, J:45302] |
Show
Allelic Composition: Spta1sph-3J/Spta1sph-3J Genetic Background: NOD.Cg-H2b Spta1sph-3J
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MP:0001082 | abnormal geniculate ganglion morphology | "malformed group of sensory neuron cell bodies associated with the facial nerve (seventh cranial nerve)" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:45302] |
Show
Allelic Composition: Spta1sph-3J/Spta1sph-3J Genetic Background: NOD.Cg-H2b Spta1sph-3J
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MP:0001092 | abnormal trigeminal ganglion morphology | "malformed group of sensory neuron cell bodies associated with the trigeminal nerve (fifth cranial nerve)" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:33038] |
Show
Allelic Composition: Spta1sph-3J/Spta1sph-3J Genetic Background: NOD.Cg-H2b Spta1sph-3J
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MP:0001096 | abnormal glossopharyngeal ganglion morphology | "malformed group of neuron cell bodies associated with the ninth cranial nerve" [MeSH:National Library of Medicine - Medical Subject Headings , 2003] |
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Allelic Composition: Spta1sph-3J/Spta1sph-3J Genetic Background: NOD.Cg-H2b Spta1sph-3J
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MP:0001100 | abnormal vagus ganglion morphology | "malformed group of sensory neuron cell bodies associated with the vagus nerve" [Stedman s Medical Dictionary:ISBN 0-683-40008-8] |
Show
Allelic Composition: Spta1sph-3J/Spta1sph-3J Genetic Background: NOD.Cg-H2b Spta1sph-3J
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MP:0001116 | small gonad | "reduced size of the testis or the ovary" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:34193] |
Show
Allelic Composition: Spta1sph-3J/Spta1sph-3J Genetic Background: NOD.Cg-H2b Spta1sph-3J
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MP:0001147 | small testis | "reduced size of the male reproductive glands" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:58959] |
Show
Allelic Composition: Alx3tm1Hubr/Alx3+ Genetic Background: involves: 129P2/OlaHsd
Allelic Composition: Rdh10tm1c(KOMP)Wtsi/Rdh10tm1c(KOMP)Wtsi,Tg(Amh-cre)8815Reb/0,Tg(RARE-Hspa1b/lacZ)12Jrt/0,Tg(Stra8-icre)1Reb/0 Genetic Background: involves: C57BL/6 * C57BL/6N * CD-1 * FVB/N * SJL
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MP:0001154 | seminiferous tubule degeneration | "a retrogressive impairment of function or destruction of the tubules in the testes where spermatogenesis occurs" [J:50844] |
Show
Allelic Composition: Alx3tm1Hubr/Alx3+ Genetic Background: involves: 129P2/OlaHsd
Allelic Composition: Rdh10tm1c(KOMP)Wtsi/Rdh10tm1c(KOMP)Wtsi,Tg(Amh-cre)8815Reb/0,Tg(Stra8-icre)1Reb/0 Genetic Background: involves: C57BL/6 * C57BL/6N * FVB/N * SJL
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MP:0001156 | abnormal spermatogenesis | "incomplete maturation or aberrant formation of the male gametes" [J:58959] |
Show
Allelic Composition: Alx3tm1Hubr/Alx3+ Genetic Background: involves: 129P2/OlaHsd
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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] |
Show
Allelic Composition: Spta1sph-3J/Spta1sph-3J Genetic Background: NOD.Cg-H2b Spta1sph-3J
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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] |
Show
Allelic Composition: Spta1sph-3J/Spta1sph-3J Genetic Background: NOD.Cg-H2b Spta1sph-3J
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MP:0001181 | absent lungs | "missing organs of respiration" [J:51966, J:50768] |
Show
Allelic Composition: Rdh10tm1.1Ics/Rdh10tm1.1Ics Genetic Background: involves: C57BL/6 * SJL
Allelic Composition: Rdh10tm2Ics/Rdh10tm2Ics Genetic Background: Not Specified
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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] |
Show
Allelic Composition: Spta1sph-3J/Spta1sph-3J Genetic Background: NOD.Cg-H2b Spta1sph-3J
Allelic Composition: Rdh10tm1.1Ics/Rdh10tm1.1Ics Genetic Background: involves: C57BL/6 * SJL
Allelic Composition: Rdh10tm2Ics/Rdh10tm2Ics Genetic Background: Not Specified
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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: Spta1sph-3J/Spta1sph-3J Genetic Background: NOD.Cg-H2b Spta1sph-3J
Allelic Composition: Rdh10tm1.1Ics/Rdh10tm1.1Ics Genetic Background: involves: C57BL/6 * SJL
Allelic Composition: Rdh10tm2Ics/Rdh10tm2Ics Genetic Background: Not Specified
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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] |
Show
Allelic Composition: Spta1sph-3J/Spta1sph-3J Genetic Background: NOD.Cg-H2b Spta1sph-3J
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MP:0001394 | circling | "repeated, compulsive movement in a circle; often associated with inner ear defects" [MGI:CLS, J:61295] |
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Allelic Composition: Rdh10tm1.1Ics/Rdh10tm1.1Ics Genetic Background: involves: C57BL/6 * SJL
Allelic Composition: Rdh10tm2Ics/Rdh10tm2Ics Genetic Background: Not Specified
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MP:0001544 | abnormal cardiovascular system physiology | "anomalous function of the blood, blood vessels, and/or the heart" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator] |
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Allelic Composition: Lin28atm1Gqda/Lin28atm1Gqda,Myf5tm3(cre)Sor/Myf5+ Genetic Background: involves: 129S4/SvJae * C57BL/6 * CD-1
Allelic Composition: Rdh10tm2Ics/Rdh10tm2Ics Genetic Background: Not Specified
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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] |
Show
Allelic Composition: Lin28atm1Gqda/Lin28atm1Gqda,Myf5tm3(cre)Sor/Myf5+ Genetic Background: involves: 129S4/SvJae * C57BL/6 * CD-1
Allelic Composition: Rdh10tm2Ics/Rdh10tm2Ics Genetic Background: Not Specified
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MP:0001680 | abnormal mesoderm development | "failure or abnormality in the formation of the mesoderm during gastrulation" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
Show
Allelic Composition: Rdh10tm1.1Ics/Rdh10tm1.1Ics Genetic Background: involves: C57BL/6 * SJL
Allelic Composition: Rdh10tm2Ics/Rdh10tm2Ics Genetic Background: Not Specified
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MP:0001698 | reduced embryo size | "smaller proportions of embryo compared to littermates" [J:61790] |
Show
Allelic Composition: Rdh10tm1a(KOMP)Wtsi/Rdh10tm1a(KOMP)Wtsi Genetic Background: involves: C57BL/6J * C57BL/6N
Allelic Composition: Rdh10tm1a(KOMP)Wtsi/Rdh10trex Genetic Background: involves: 129S1/Sv * C57BL/6J * C57BL/6N
Allelic Composition: Rdh10tm1d(KOMP)Wtsi/Rdh10tm1d(KOMP)Wtsi Genetic Background: involves: 129S4/SvJaeSor * C57BL/6J * C57BL/6N
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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: Umodtm1Xrw/Umod+ Genetic Background: B6.129S6-Umodtm1Xrw
Allelic Composition: Rdh10tm1d(KOMP)Wtsi/Rdh10tm1d(KOMP)Wtsi Genetic Background: involves: 129S4/SvJaeSor * C57BL/6J * C57BL/6N
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MP:0001701 | incomplete embryo turning | "arrest of the axial rotation of the germ layers of the embryo during the primitive streak/early somite stage (E8.5-E9.5)" [J:62571] |
Show
Allelic Composition: Rdh10tm1.1Ics/Rdh10tm1.1Ics Genetic Background: involves: C57BL/6 * SJL
Allelic Composition: Rdh10tm2Ics/Rdh10tm2Ics Genetic Background: Not Specified
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MP:0001730 | embryonic growth arrest | "the cessation of development beyond a particular stage" [J:17509] |
Show
Allelic Composition: Rdh10tm1a(KOMP)Wtsi/Rdh10trex Genetic Background: involves: 129S1/Sv * C57BL/6J * C57BL/6N
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MP:0001914 | hemorrhage | "loss of blood from the vascular compartment to the exterior or into nonvascular body space as a result of rupture or severance of the blood vessels" [Stedman s Medical Dictionary, 27th edition:ISBN 0-683-40008-8] |
Show
Allelic Composition: Spta1sph-3J/Spta1sph-3J Genetic Background: NOD.Cg-H2b Spta1sph-3J
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MP:0001922 | reduced male fertility | "reduced ability of male to produce live offspring" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:61340] |
Show
Allelic Composition: Alx3tm1Hubr/Alx3+ Genetic Background: involves: 129P2/OlaHsd
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MP:0002085 | abnormal embryonic tissue morphology | "structural abnormality or development of any embryonic tissue resulting in morphological abnormality" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
Show
Allelic Composition: Rdh10tm1a(KOMP)Wtsi/Rdh10tm1a(KOMP)Wtsi Genetic Background: involves: C57BL/6J * C57BL/6N
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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] |
Show
Allelic Composition: Rdh10m366Asp/Rdh10m366Asp Genetic Background: involves: C57BL/6J
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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] |
Show
Allelic Composition: Rdh10m366Asp/Rdh10m366Asp Genetic Background: involves: C57BL/6J
Allelic Composition: Rdh10tm1.1Ics/Rdh10tm1.1Ics Genetic Background: involves: C57BL/6 * SJL
Allelic Composition: Rdh10tm2Ics/Rdh10tm2Ics Genetic Background: Not Specified
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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] |
Show
Allelic Composition: Lin28atm1Gqda/Lin28atm1Gqda,Myf5tm3(cre)Sor/Myf5+ Genetic Background: involves: 129S4/SvJae * C57BL/6 * CD-1
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MP:0002216 | abnormal seminiferous tubule morphology | "malformation of the tubules in the testes where spermatogenesis occurs" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
Show
Allelic Composition: Alx3tm1Hubr/Alx3+ Genetic Background: involves: 129P2/OlaHsd
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MP:0002544 | brachydactyly | "abnormally short digits" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8] |
Show
Allelic Composition: Rdh10tm1.1Ics/Rdh10tm1.1Ics Genetic Background: involves: C57BL/6 * SJL
Allelic Composition: Rdh10tm2Ics/Rdh10tm2Ics Genetic Background: Not Specified
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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] |
Show
Allelic Composition: Rdh10tm1.1Ics/Rdh10tm1.1Ics Genetic Background: involves: C57BL/6 * SJL
Allelic Composition: Rdh10tm2Ics/Rdh10tm2Ics Genetic Background: Not Specified
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MP:0002691 | small stomach | "reduced size of the stomach" [J:77398, dlb:Donna Burkart , Mouse Genome Informatics Curator] |
Show
Allelic Composition: Spta1sph-3J/Spta1sph-3J Genetic Background: NOD.Cg-H2b Spta1sph-3J
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MP:0002884 | abnormal branchial arches | "malformation or anomaly in the transient structures of the embryo that develop into regions of the head, neck and ears" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
Show
Allelic Composition: Spta1sph-3J/Spta1sph-3J Genetic Background: NOD.Cg-H2b Spta1sph-3J
Allelic Composition: Rdh10tm1.1Ics/Rdh10tm1.1Ics Genetic Background: involves: C57BL/6 * SJL
Allelic Composition: Rdh10tm2Ics/Rdh10tm2Ics Genetic Background: Not Specified
Allelic Composition: Rdh10trex/Rdh10trex Genetic Background: involves: 129S1/Sv * C57BL/6
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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] |
Show
Allelic Composition: Spta1sph-3J/Spta1sph-3J Genetic Background: NOD.Cg-H2b Spta1sph-3J
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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] |
Show
Allelic Composition: Rdh10tm1.1Ics/Rdh10tm1.1Ics Genetic Background: involves: C57BL/6 * SJL
Allelic Composition: Rdh10tm2Ics/Rdh10tm2Ics Genetic Background: Not Specified
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MP:0003655 | absent pancreas | "absence of the organ that secretes pancreatic juice into the duodenum and secretes glucagon and insulin into the bloodstream" [anna:Anna Anagnostopoulos, Mouse Genome Informatics Curator, J:20779] |
Show
Allelic Composition: Spta1sph-3J/Spta1sph-3J Genetic Background: NOD.Cg-H2b Spta1sph-3J
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MP:0003698 | abnormal male reproductive system physiology | "anomaly in the function of the male organs associated with producing offspring " [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
Show
Allelic Composition: Alx3tm1Hubr/Alx3+ Genetic Background: involves: 129P2/OlaHsd
Allelic Composition: Rdh10tm1c(KOMP)Wtsi/Rdh10tm1c(KOMP)Wtsi,Tg(Amh-cre)8815Reb/0,Tg(Stra8-icre)1Reb/0 Genetic Background: involves: C57BL/6 * C57BL/6N * FVB/N * SJL
Allelic Composition: Rdh10tm1c(KOMP)Wtsi/Rdh10tm1c(KOMP)Wtsi,Tg(Amh-cre)8815Reb/0,Tg(RARE-Hspa1b/lacZ)12Jrt/0,Tg(Stra8-icre)1Reb/0 Genetic Background: involves: C57BL/6 * C57BL/6N * CD-1 * FVB/N * SJL
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MP:0003703 | abnormal vestibulocochlear ganglion morphology | "malformed group of neuron cell bodies associated with the eighth cranial nerve during embryogenesis; splits in later development to form the cochlear and vestibular ganglia" [smb:Susan M Bello, Mouse Genome Informatics Curator] |
Show
Allelic Composition: Spta1sph-3J/Spta1sph-3J Genetic Background: NOD.Cg-H2b Spta1sph-3J
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MP:0003874 | absent branchial arches | "missing the transient structures of the embryo that develop into regions of the head, neck and ears" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator, anna:Anna Anagnostopoulos, Mouse Genome Informatics Curator] |
Show
Allelic Composition: Spta1sph-3J/Spta1sph-3J Genetic Background: NOD.Cg-H2b Spta1sph-3J
Allelic Composition: Rdh10tm1a(KOMP)Wtsi/Rdh10tm1a(KOMP)Wtsi Genetic Background: involves: C57BL/6J * C57BL/6N
Allelic Composition: Rdh10trex/Rdh10trex Genetic Background: involves: 129S1/Sv * 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] |
Show
Allelic Composition: Rdh10tm1a(KOMP)Wtsi/Rdh10tm1a(KOMP)Wtsi Genetic Background: involves: C57BL/6J * C57BL/6N
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MP:0003935 | abnormal craniofacial development | "anomaly in the process of forming the face and/or cranium" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
Show
Allelic Composition: Rdh10tm1.1Ics/Rdh10tm1.1Ics Genetic Background: involves: C57BL/6 * SJL
Allelic Composition: Rdh10tm2Ics/Rdh10tm2Ics Genetic Background: Not Specified
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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] |
Show
Allelic Composition: Spta1sph-3J/Spta1sph-3J Genetic Background: NOD.Cg-H2b Spta1sph-3J
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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: Rdh10tm1.1Ics/Rdh10tm1.1Ics Genetic Background: involves: C57BL/6 * SJL
Allelic Composition: Rdh10tm2Ics/Rdh10tm2Ics Genetic Background: Not Specified
Allelic Composition: Rdh10tm1a(KOMP)Wtsi/Rdh10tm1a(KOMP)Wtsi Genetic Background: involves: C57BL/6J * C57BL/6N
Allelic Composition: Rdh10tm1d(KOMP)Wtsi/Rdh10tm1d(KOMP)Wtsi Genetic Background: involves: 129S4/SvJaeSor * C57BL/6J * C57BL/6N
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MP:0004073 | caudal body truncation | "caudal part of body truncated with anterior portion relatively normal" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator] |
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Allelic Composition: Rdh10tm1.1Ics/Rdh10tm1.1Ics Genetic Background: involves: C57BL/6 * SJL
Allelic Composition: Rdh10tm2Ics/Rdh10tm2Ics Genetic Background: Not Specified
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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: Rdh10tm1a(KOMP)Wtsi/Rdh10tm1a(KOMP)Wtsi Genetic Background: involves: C57BL/6J * C57BL/6N
Allelic Composition: Rdh10tm1d(KOMP)Wtsi/Rdh10tm1d(KOMP)Wtsi Genetic Background: involves: 129S4/SvJaeSor * C57BL/6J * C57BL/6N
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MP:0004310 | small otic vesicle | "reduced size of the simple epithelial sac formed from the otic placode that gives rise to the structures of the inner ear" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"] |
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Allelic Composition: Spta1sph-3J/Spta1sph-3J Genetic Background: NOD.Cg-H2b Spta1sph-3J
Allelic Composition: Rdh10tm1.1Ics/Rdh10tm1.1Ics Genetic Background: involves: C57BL/6 * SJL
Allelic Composition: Rdh10tm2Ics/Rdh10tm2Ics Genetic Background: Not Specified
Allelic Composition: Rdh10tm1a(KOMP)Wtsi/Rdh10tm1a(KOMP)Wtsi Genetic Background: involves: C57BL/6J * C57BL/6N
Allelic Composition: Rdh10tm1d(KOMP)Wtsi/Rdh10tm1d(KOMP)Wtsi Genetic Background: involves: 129S4/SvJaeSor * C57BL/6J * C57BL/6N
Allelic Composition: Rdh10trex/Rdh10trex Genetic Background: involves: 129S1/Sv * C57BL/6
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MP:0004787 | abnormal dorsal aorta morphology | "any structural anomaly of the paired arterial structures of the embryo that supplies each developing somite via efferent segmental arteries; the dorsal aortae articulate with the umbilical arteries, which return mixed blood to the villi of the chorion for reoxygenation" [ISBN:0-914294-08-3 "Gray s Anatomy"] |
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Allelic Composition: Spta1sph-3J/Spta1sph-3J Genetic Background: NOD.Cg-H2b Spta1sph-3J
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MP:0004852 | decreased testis weight | "reduced average weight of the male reproductive glands" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Alx3tm1Hubr/Alx3+ Genetic Background: involves: 129P2/OlaHsd
Allelic Composition: Rdh10tm1c(KOMP)Wtsi/Rdh10tm1c(KOMP)Wtsi,Tg(Amh-cre)8815Reb/0,Tg(Stra8-icre)1Reb/0 Genetic Background: involves: C57BL/6 * C57BL/6N * FVB/N * SJL
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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: Spta1sph-3J/Spta1sph-3J Genetic Background: NOD.Cg-H2b Spta1sph-3J
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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: Spta1sph-3J/Spta1sph-3J Genetic Background: NOD.Cg-H2b Spta1sph-3J
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MP:0006108 | abnormal hindbrain development | "anomaly in the formation or pattering of the caudal region of the brain" [smb:Susan M Bello, Mouse Genome Informatics Curator, J:93573] |
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Allelic Composition: Rdh10tm1.1Ics/Rdh10tm1.1Ics Genetic Background: involves: C57BL/6 * SJL
Allelic Composition: Rdh10tm2Ics/Rdh10tm2Ics Genetic Background: Not Specified
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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: Spta1sph-3J/Spta1sph-3J Genetic Background: NOD.Cg-H2b Spta1sph-3J
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MP:0006254 | thin cerebral cortex | "decreased depth of the mantle covering the surface of the cerebral hemispheres" [smb:Susan M Bello, Mouse Genome Informatics Curator, J:84683] |
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Allelic Composition: Tnftm1Ljo/Tnftm1Ljo Genetic Background: B6.129S1-Tnftm1Ljo
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MP:0006280 | abnormal digit development | "anomaly in the formation of the digits" [J:70592, MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator"] |
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Allelic Composition: Spta1sph-3J/Spta1sph-3J Genetic Background: NOD.Cg-H2b Spta1sph-3J
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MP:0006292 | abnormal olfactory placode morphology | "any structural abnormality in the paired ectodermal placodes that come to lie in the bottom of the olfactory pits as the pits are deepened by the growth of the surrounding medial and lateral nasal processes" [J:62024, MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"] |
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Allelic Composition: Spta1sph-3J/Spta1sph-3J Genetic Background: NOD.Cg-H2b Spta1sph-3J
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MP:0006339 | abnormal third branchial arch morphology | "anomaly in the structure of the third are which contributes to the development of the hyoid bone, stylopharyngeus muscle, inferior parathyroid gland, and thymus" [MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator"] |
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Allelic Composition: Spta1sph-3J/Spta1sph-3J Genetic Background: NOD.Cg-H2b Spta1sph-3J
Allelic Composition: Rdh10trex/Rdh10trex Genetic Background: involves: 129S1/Sv * C57BL/6
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MP:0006340 | abnormal fourth branchial arch morphology | "anomaly in the structure of the fourth arch which contributes to development of the cartilage of the larynx, laryngeal, pharyngeal, and soft palate muscles, superior parathyroid gland, and C-cells of the thymus" [MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator", zillmusom:http://musom.marshall.edu/anatomy/grosshom/z_devbranc.html] |
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Allelic Composition: Rdh10trex/Rdh10trex Genetic Background: involves: 129S1/Sv * C57BL/6
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MP:0006347 | abnormal sixth branchial arch morphology | "anomaly in the structure of the sixth arch which contributes to the development of the sternocleidomastoid and trapezius muscles" [MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator", zillmusom:http://musom.marshall.edu/anatomy/grosshom/z_devbranc.html] |
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Allelic Composition: Rdh10trex/Rdh10trex Genetic Background: involves: 129S1/Sv * C57BL/6
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MP:0006378 | abnormal spermatogonia morphology | "anomaly in the number, structure or development of the large unspecialized male germ cells that give rise to spermatocytes" [ISBN:0-8036-0655-99 "Taber s Cyclopedic Medical Dictionary, 19th edition", MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator"] |
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Allelic Composition: Rdh10tm1c(KOMP)Wtsi/Rdh10tm1c(KOMP)Wtsi,Tg(Amh-cre)8815Reb/0,Tg(Stra8-icre)1Reb/0 Genetic Background: involves: C57BL/6 * C57BL/6N * FVB/N * SJL
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MP:0008261 | arrest of male meiosis | "cessation of the progression of the process of nuclear division that results in sperm with one half the normal chromosome number of the original cell" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"] |
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Allelic Composition: Rdh10tm1c(KOMP)Wtsi/Rdh10tm1c(KOMP)Wtsi,Tg(Amh-cre)8815Reb/0,Tg(Stra8-icre)1Reb/0 Genetic Background: involves: C57BL/6 * C57BL/6N * FVB/N * SJL
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MP:0008797 | facial cleft | "a cleft resulting from incomplete merging or fusion of any of the embryonic facial processes that normally unite to form the face" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Spta1sph-3J/Spta1sph-3J Genetic Background: NOD.Cg-H2b Spta1sph-3J
Allelic Composition: Rdh10tm1.1Ics/Rdh10tm1.1Ics Genetic Background: involves: C57BL/6 * SJL
Allelic Composition: Rdh10tm2Ics/Rdh10tm2Ics Genetic Background: Not Specified
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MP:0008986 | abnormal liver parenchyma morphology | "any structural anomaly of the functional units of the liver including the lobules" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Spta1sph-3J/Spta1sph-3J Genetic Background: NOD.Cg-H2b Spta1sph-3J
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MP:0009111 | pancreas hypoplasia | "underdevelopment or reduced size of the pancreas, usually due to a reduced number of cells" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Rdh10tm1.1Ics/Rdh10tm1.1Ics Genetic Background: involves: C57BL/6 * SJL
Allelic Composition: Rdh10tm2Ics/Rdh10tm2Ics Genetic Background: Not Specified
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MP:0009705 | abnormal midgut morphology | "any structural anomaly of the portion of the embryonic gut between the foregut and the hindgut, which originally is open to the yolk sac" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"] |
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Allelic Composition: Spta1sph-3J/Spta1sph-3J Genetic Background: NOD.Cg-H2b Spta1sph-3J
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MP:0009806 | abnormal otic vesicle morphology | "any structural anomaly of the paired sacs of invaginated ectoderm that develop into the membraneous labyrinth of the inner ear" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"] |
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Allelic Composition: Spta1sph-3J/Spta1sph-3J Genetic Background: NOD.Cg-H2b Spta1sph-3J
Allelic Composition: Rdh10tm1.1Ics/Rdh10tm1.1Ics Genetic Background: involves: C57BL/6 * SJL
Allelic Composition: Rdh10tm2Ics/Rdh10tm2Ics Genetic Background: Not Specified
Allelic Composition: Rdh10trex/Rdh10trex Genetic Background: involves: 129S1/Sv * C57BL/6
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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: Spta1sph-3J/Spta1sph-3J Genetic Background: NOD.Cg-H2b Spta1sph-3J
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MP:0009902 | abnormal lateral nasal prominence morphology | "any structural anomaly of the lateral area of the two branches of a horseshoe-shaped mesenchymal swelling in the future nasal region of the embryo; it separates the olfactory pit from the developing eye and the ala of the nose/snout develops from it" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"] |
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Allelic Composition: Spta1sph-3J/Spta1sph-3J Genetic Background: NOD.Cg-H2b Spta1sph-3J
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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: Spta1sph-3J/Spta1sph-3J Genetic Background: NOD.Cg-H2b Spta1sph-3J
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MP:0010356 | abnormal second branchial arch artery morphology | "any structural anomaly of the vessels formed within the second pair of branchial arches in embryogenesis" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Spta1sph-3J/Spta1sph-3J Genetic Background: NOD.Cg-H2b Spta1sph-3J
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MP:0010642 | absent third branchial arch | "absence of the structure of the third are which contributes to the development of the hyoid bone, stylopharyngeus muscle, inferior parathyroid gland, and thymus" [MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator"] |
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Allelic Composition: Rdh10trex/Rdh10trex Genetic Background: involves: 129S1/Sv * C57BL/6
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MP:0010643 | absent fourth branchial arch | "absence of the structure of the fourth arch which contributes to development of the cartilage of the larynx, laryngeal, pharyngeal, and soft palate muscles, superior parathyroid gland, and C-cells of the thymus" [MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator"] |
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Allelic Composition: Spta1sph-3J/Spta1sph-3J Genetic Background: NOD.Cg-H2b Spta1sph-3J
Allelic Composition: Rdh10trex/Rdh10trex Genetic Background: involves: 129S1/Sv * C57BL/6
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MP:0010644 | absent sixth branchial arch | "absence of the structure of the sixth arch which contributes to the development of the sternocleidomastoid and trapezius muscles" [MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator"] |
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Allelic Composition: Rdh10trex/Rdh10trex Genetic Background: involves: 129S1/Sv * C57BL/6
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MP:0010707 | decreased ventral retina size | "decreasd size of the ventral portion of the retina" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator", PMID:7923367] |
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Allelic Composition: Rdh10tm1.1Ics/Rdh10tm1.1Ics Genetic Background: involves: C57BL/6 * SJL
Allelic Composition: Rdh10tm2Ics/Rdh10tm2Ics Genetic Background: Not Specified
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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: Spta1sph-3J/Spta1sph-3J Genetic Background: NOD.Cg-H2b Spta1sph-3J
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MP:0010940 | abnormal maxillary prominence morphology | |
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Allelic Composition: Spta1sph-3J/Spta1sph-3J Genetic Background: NOD.Cg-H2b Spta1sph-3J
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MP:0011026 | impaired branching involved in trachea morphogenesis | |
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Allelic Composition: Spta1sph-3J/Spta1sph-3J Genetic Background: NOD.Cg-H2b Spta1sph-3J
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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: Spta1sph-3J/Spta1sph-3J Genetic Background: NOD.Cg-H2b Spta1sph-3J
Allelic Composition: Rdh10tm1.1Ics/Rdh10tm1.1Ics Genetic Background: involves: C57BL/6 * SJL
Allelic Composition: Rdh10tm2Ics/Rdh10tm2Ics Genetic Background: Not Specified
Allelic Composition: Rdh10tm1d(KOMP)Wtsi/Rdh10tm1d(KOMP)Wtsi Genetic Background: involves: 129S4/SvJaeSor * C57BL/6J * C57BL/6N
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MP:0011111 | complete lethality during fetal growth through weaning | "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 weaning age (Mus: E14 to approximately 3 weeks of age)" [MGI:csmith] |
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Allelic Composition: Rdh10tm1.1Ics/Rdh10tm1.1Ics Genetic Background: involves: C57BL/6 * SJL
Allelic Composition: Rdh10tm2Ics/Rdh10tm2Ics Genetic Background: Not Specified
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MP:0011233 | abnormal vitamin A metabolism | "altered ability to metabolize any of the vitamin A compounds, retinol, retinal (retinaldehyde) and retinoic acid; animals can not synthesize vitamin A de novo, but form it through oxidative cleavage of carotenoids supplied in the diet" [GO:0035238] |
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Allelic Composition: Rdh10tm1d(KOMP)Wtsi/Rdh10tm1d(KOMP)Wtsi Genetic Background: involves: 129S4/SvJaeSor * C57BL/6J * C57BL/6N
Allelic Composition: Rdh10trex/Rdh10trex Genetic Background: involves: 129S1/Sv * C57BL/6
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MP:0011364 | abnormal metanephros morphology | "any structural anomaly of the primordium of the permanent kidney, which develops later than and caudal to the mesonephros, from the mesonephric duct and nephrogenic cord; the metanephros is an endocrine and metabolic organ that filters the blood and excretes the end products of body metabolism in the form of urine" [GO:0001656] |
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Allelic Composition: Spta1sph-3J/Spta1sph-3J Genetic Background: NOD.Cg-H2b Spta1sph-3J
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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: Rdh10tm1a(KOMP)Wtsi/Rdh10tm1a(KOMP)Wtsi Genetic Background: involves: C57BL/6J * C57BL/6N
Allelic Composition: Rdh10tm1a(KOMP)Wtsi/Rdh10trex Genetic Background: involves: 129S1/Sv * C57BL/6J * C57BL/6N
Allelic Composition: Rdh10tm1d(KOMP)Wtsi/Rdh10tm1d(KOMP)Wtsi Genetic Background: involves: 129S4/SvJaeSor * C57BL/6J * C57BL/6N
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MP:0012247 | absent cornea | "absence of the transparent anterior portion of the fibrous coat of the eye that serves as the chief refractory structure" [MGI:anna] |
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Allelic Composition: Spta1sph-3J/Spta1sph-3J Genetic Background: NOD.Cg-H2b Spta1sph-3J
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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: Rdh10trex/Rdh10trex Genetic Background: involves: 129S1/Sv * C57BL/6
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MP:0013164 | abnormal forelimb bud morphology | "any structural anomaly of the limb bud that develops into a forelimb (usually the arm or front limb in mammalian species)" [MGI:anna] |
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Allelic Composition: Spta1sph-3J/Spta1sph-3J Genetic Background: NOD.Cg-H2b Spta1sph-3J
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MP:0013166 | small forelimb buds | "reduced size of the limb bud that normally develops into a forelimb (usually the arm or front limb in mammalian species)" [MGI:anna] |
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Allelic Composition: Rdh10tm1.1Ics/Rdh10tm1.1Ics Genetic Background: involves: C57BL/6 * SJL
Allelic Composition: Rdh10tm2Ics/Rdh10tm2Ics Genetic Background: Not Specified
Allelic Composition: Rdh10trex/Rdh10trex Genetic Background: involves: 129S1/Sv * C57BL/6
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MP:0013241 | embryo tissue necrosis | "morphological changes resulting from pathological death of some or all embryo tissue; usually due to irreversible damage" [MGI:csmith] |
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Allelic Composition: Rdh10tm1.1Ics/Rdh10tm1.1Ics Genetic Background: involves: C57BL/6 * SJL
Allelic Composition: Rdh10tm2Ics/Rdh10tm2Ics Genetic Background: Not Specified
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MP:0013817 | absent nasal cavity | "absence of the cavity of the respiratory tract that extends from the nares to the pharynx; the nasal cavity is lined with ciliated mucosa" [MESH:A04.531.449] |
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Allelic Composition: Spta1sph-3J/Spta1sph-3J Genetic Background: NOD.Cg-H2b Spta1sph-3J
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MP:0020350 | fused pharyngeal arches | "failure of two or more arches to fully separate" [ORCID: orcid.org/0000-0003-4606-0597, PMID:22319578] |
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Allelic Composition: Spta1sph-3J/Spta1sph-3J Genetic Background: NOD.Cg-H2b Spta1sph-3J
Allelic Composition: Rdh10trex/Rdh10trex Genetic Background: involves: 129S1/Sv * 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: Spta1sph-3J/Spta1sph-3J Genetic Background: NOD.Cg-H2b Spta1sph-3J
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MP:0030334 | absent sixth pharyngeal arch artery | "failure to develop or absence of the sixth pharyngeal arch artery" [MGI:anna] |
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Allelic Composition: Spta1sph-3J/Spta1sph-3J Genetic Background: NOD.Cg-H2b Spta1sph-3J
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MP:0030335 | absent third pharyngeal arch artery | "failure to develop or absence of the third pharyngeal arch artery" [MGI:anna] |
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Allelic Composition: Spta1sph-3J/Spta1sph-3J Genetic Background: NOD.Cg-H2b Spta1sph-3J
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