ENSMUSG00000025921


Mus musculus

Features
Gene ID: ENSMUSG00000025921
  
Biological name :Rdh10
  
Synonyms : Q8VCH7 / Rdh10 / Retinol dehydrogenase 10
  
Possible biological names infered from orthology : Q8IZV5
  
Species: Mus musculus
  
Chr. number: 1
Strand: 1
Band: A3
Gene start: 16105774
Gene end: 16133734
  
Corresponding Affymetrix probe sets: 10344952 (MoGene1.0st)   1426968_a_at (Mouse Genome 430 2.0 Array)   1460632_at (Mouse Genome 430 2.0 Array)   
  
Cross references: Ensembl peptide - ENSMUSP00000027053
NCBI entrez gene - 98711     See in Manteia.
MGI - MGI:1924238
RefSeq - NM_133832
RefSeq Peptide - NP_598593
swissprot - Q8VCH7
Ensembl - ENSMUSG00000025921
  
See expression report in BioGPS
See gene description in Wikigenes
See co-cited genes in PubMed


Ortholog prediction (from Ensembl)
Ortholog nameID Species
 Q7T2D1ENSDARG00000012369Danio rerio
 rdh10aENSDARG00000058730Danio rerio
 RDH10ENSGALG00000034346Gallus gallus
 RDH10ENSG00000121039Homo sapiens


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
Q7TQA3 / Sdr16c5 / Epidermal retinol dehydrogenase 2 / Q8N3Y7* / short chain dehydrogenase/reductase family 16C member 5*ENSMUSG0000002823641
Q05A13 / Sdr16c6 / Short-chain dehydrogenase/reductase family 16C member 6 ENSMUSG0000007101939
Q9EQ06 / Hsd17b11 / hydroxysteroid (17-beta) dehydrogenase 11 / Q8NBQ5*ENSMUSG0000002931135
Dhrs3 / O88876 / Short-chain dehydrogenase/reductase 3 / O75911* / dehydrogenase/reductase 3*ENSMUSG0000006602633
Q8VCR2 / Hsd17b13 / hydroxysteroid (17-beta) dehydrogenase 13 / Q7Z5P4*ENSMUSG0000003452832


Protein motifs (from Interpro)
Interpro ID Name
 IPR002347  Short-chain dehydrogenase/reductase SDR
 IPR020904  Short-chain dehydrogenase/reductase, conserved site
 IPR032970  Retinol dehydrogenase 10
 IPR036291  NAD(P)-binding domain superfamily


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0001656 metanephros development IMP
 biological_processGO:0001701 in utero embryonic development IMP
 biological_processGO:0002138 retinoic acid biosynthetic process IMP
 biological_processGO:0007601 visual perception IEA
 biological_processGO:0008406 gonad development IMP
 biological_processGO:0009887 animal organ morphogenesis IMP
 biological_processGO:0014032 neural crest cell development IMP
 biological_processGO:0031076 embryonic camera-type eye development IMP
 biological_processGO:0035115 embryonic forelimb morphogenesis IMP
 biological_processGO:0042572 retinol metabolic process IEA
 biological_processGO:0042574 retinal metabolic process IEA
 biological_processGO:0043583 ear development IMP
 biological_processGO:0043584 nose development IMP
 biological_processGO:0048568 embryonic organ development IMP
 biological_processGO:0048703 embryonic viscerocranium morphogenesis IMP
 biological_processGO:0055114 oxidation-reduction process IEA
 biological_processGO:0060431 primary lung bud formation IMP
 biological_processGO:0060449 bud elongation involved in lung branching IMP
 cellular_componentGO:0005737 cytoplasm IEA
 cellular_componentGO:0005783 endoplasmic reticulum IEA
 cellular_componentGO:0005789 endoplasmic reticulum membrane IEA
 cellular_componentGO:0016020 membrane IDA
 cellular_componentGO:0016021 integral component of membrane ISO
 cellular_componentGO:0031090 organelle membrane IEA
 cellular_componentGO:0043231 intracellular membrane-bounded organelle IEA
 cellular_componentGO:0044297 cell body IEA
 molecular_functionGO:0004745 retinol dehydrogenase activity IEA
 molecular_functionGO:0016491 oxidoreductase activity IEA
 molecular_functionGO:0052650 NADP-retinol dehydrogenase activity IEA


Pathways (from Reactome)
Pathway description
The canonical retinoid cycle in rods (twilight vision)
RA biosynthesis pathway


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 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

 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

 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

 MP:0000270 abnormal heart tube morphology "malformed embryonic heart " [J:37888]
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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

 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: Spta1sph-3J/Spta1sph-3J
Genetic Background: NOD.Cg-H2b Spta1sph-3J

Allelic Composition: Rdh10m366Asp/Rdh10m366Asp
Genetic Background: involves: C57BL/6J

 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]
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Allelic Composition: Rdh10tm1.1Ics/Rdh10tm1.1Ics
Genetic Background: involves: C57BL/6 * SJL

Allelic Composition: Rdh10tm2Ics/Rdh10tm2Ics
Genetic Background: Not Specified

 MP:0000477 abnormal intestine morphology "malformation of the digestive tube passing from the stomach to the anus" [J:48968]
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Allelic Composition: Rdh10tm1.1Ics/Rdh10tm1.1Ics
Genetic Background: involves: C57BL/6 * SJL

Allelic Composition: Rdh10tm2Ics/Rdh10tm2Ics
Genetic Background: Not Specified

 MP:0000550 abnormal forelimb morphology "malformation of the entire anterior extremities" [MGI:tc]
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Allelic Composition: Spta1sph-3J/Spta1sph-3J
Genetic Background: NOD.Cg-H2b Spta1sph-3J

 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

 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: Rdh10tm1.1Ics/Rdh10tm1.1Ics
Genetic Background: involves: C57BL/6 * SJL

Allelic Composition: Rdh10tm2Ics/Rdh10tm2Ics
Genetic Background: Not Specified

 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

 MP:0000600 liver hypoplasia "reduced size of liver due to decreased cell number " [J:57631]
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Allelic Composition: Rdh10tm1.1Ics/Rdh10tm1.1Ics
Genetic Background: involves: C57BL/6 * SJL

Allelic Composition: Rdh10tm2Ics/Rdh10tm2Ics
Genetic Background: Not Specified

 MP:0000601 small liver "reduced size of the liver" [J:23170]
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Allelic Composition: Spta1sph-3J/Spta1sph-3J
Genetic Background: NOD.Cg-H2b Spta1sph-3J

 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: Rdh10m366Asp/Rdh10m366Asp
Genetic Background: involves: C57BL/6J

 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]
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Allelic Composition: Rdh10m366Asp/Rdh10m366Asp
Genetic Background: involves: C57BL/6J

 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]
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Allelic Composition: Spta1sph-3J/Spta1sph-3J
Genetic Background: NOD.Cg-H2b Spta1sph-3J

 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]
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Allelic Composition: Spta1sph-3J/Spta1sph-3J
Genetic Background: NOD.Cg-H2b Spta1sph-3J

 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]
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Allelic Composition: Spta1sph-3J/Spta1sph-3J
Genetic Background: NOD.Cg-H2b Spta1sph-3J

 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

 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]
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Allelic Composition: Spta1sph-3J/Spta1sph-3J
Genetic Background: NOD.Cg-H2b Spta1sph-3J

 MP:0001116 small gonad "reduced size of the testis or the ovary" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:34193]
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Allelic Composition: Spta1sph-3J/Spta1sph-3J
Genetic Background: NOD.Cg-H2b Spta1sph-3J

 MP:0001147 small testis "reduced size of the male reproductive glands" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:58959]
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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(RARE-Hspa1b/lacZ)12Jrt/0,Tg(Stra8-icre)1Reb/0
Genetic Background: involves: C57BL/6 * C57BL/6N * CD-1 * FVB/N * SJL

 MP:0001154 seminiferous tubule degeneration "a retrogressive impairment of function or destruction of the tubules in the testes where spermatogenesis occurs" [J:50844]
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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

 MP:0001156 abnormal spermatogenesis "incomplete maturation or aberrant formation of the male gametes" [J:58959]
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Allelic Composition: Alx3tm1Hubr/Alx3+
Genetic Background: involves: 129P2/OlaHsd

 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: Spta1sph-3J/Spta1sph-3J
Genetic Background: NOD.Cg-H2b Spta1sph-3J

 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: Spta1sph-3J/Spta1sph-3J
Genetic Background: NOD.Cg-H2b Spta1sph-3J

 MP:0001181 absent lungs "missing organs of respiration" [J:51966, J:50768]
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Allelic Composition: Rdh10tm1.1Ics/Rdh10tm1.1Ics
Genetic Background: involves: C57BL/6 * SJL

Allelic Composition: Rdh10tm2Ics/Rdh10tm2Ics
Genetic Background: Not Specified

 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

 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]
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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

 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: Spta1sph-3J/Spta1sph-3J
Genetic Background: NOD.Cg-H2b Spta1sph-3J

 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

 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

 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: Lin28atm1Gqda/Lin28atm1Gqda,Myf5tm3(cre)Sor/Myf5+
Genetic Background: involves: 129S4/SvJae * C57BL/6 * CD-1

Allelic Composition: Rdh10tm2Ics/Rdh10tm2Ics
Genetic Background: Not Specified

 MP:0001680 abnormal mesoderm development "failure or abnormality in the formation of the mesoderm during gastrulation" [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

 MP:0001698 reduced embryo size "smaller proportions of embryo compared to littermates" [J:61790]
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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

 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

 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]
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Allelic Composition: Rdh10tm1.1Ics/Rdh10tm1.1Ics
Genetic Background: involves: C57BL/6 * SJL

Allelic Composition: Rdh10tm2Ics/Rdh10tm2Ics
Genetic Background: Not Specified

 MP:0001730 embryonic growth arrest "the cessation of development beyond a particular stage" [J:17509]
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Allelic Composition: Rdh10tm1a(KOMP)Wtsi/Rdh10trex
Genetic Background: involves: 129S1/Sv * C57BL/6J * C57BL/6N

 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]
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Allelic Composition: Spta1sph-3J/Spta1sph-3J
Genetic Background: NOD.Cg-H2b Spta1sph-3J

 MP:0001922 reduced male fertility "reduced ability of male to produce live offspring" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:61340]
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Allelic Composition: Alx3tm1Hubr/Alx3+
Genetic Background: involves: 129P2/OlaHsd

 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]
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Allelic Composition: Rdh10tm1a(KOMP)Wtsi/Rdh10tm1a(KOMP)Wtsi
Genetic Background: involves: C57BL/6J * C57BL/6N

 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: Rdh10m366Asp/Rdh10m366Asp
Genetic Background: involves: C57BL/6J

 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: 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

 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: Lin28atm1Gqda/Lin28atm1Gqda,Myf5tm3(cre)Sor/Myf5+
Genetic Background: involves: 129S4/SvJae * C57BL/6 * CD-1

 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]
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Allelic Composition: Alx3tm1Hubr/Alx3+
Genetic Background: involves: 129P2/OlaHsd

 MP:0002544 brachydactyly "abnormally short digits" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8]
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Allelic Composition: Rdh10tm1.1Ics/Rdh10tm1.1Ics
Genetic Background: involves: C57BL/6 * SJL

Allelic Composition: Rdh10tm2Ics/Rdh10tm2Ics
Genetic Background: Not Specified

 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: Rdh10tm1.1Ics/Rdh10tm1.1Ics
Genetic Background: involves: C57BL/6 * SJL

Allelic Composition: Rdh10tm2Ics/Rdh10tm2Ics
Genetic Background: Not Specified

 MP:0002691 small stomach "reduced size of the stomach" [J:77398, dlb:Donna Burkart , Mouse Genome Informatics Curator]
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Allelic Composition: Spta1sph-3J/Spta1sph-3J
Genetic Background: NOD.Cg-H2b Spta1sph-3J

 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]
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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

 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: Spta1sph-3J/Spta1sph-3J
Genetic Background: NOD.Cg-H2b Spta1sph-3J

 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: Rdh10tm1.1Ics/Rdh10tm1.1Ics
Genetic Background: involves: C57BL/6 * SJL

Allelic Composition: Rdh10tm2Ics/Rdh10tm2Ics
Genetic Background: Not Specified

 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]
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Allelic Composition: Spta1sph-3J/Spta1sph-3J
Genetic Background: NOD.Cg-H2b Spta1sph-3J

 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]
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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

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

 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]
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Allelic Composition: Spta1sph-3J/Spta1sph-3J
Genetic Background: NOD.Cg-H2b Spta1sph-3J

 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]
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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

 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: Rdh10tm1a(KOMP)Wtsi/Rdh10tm1a(KOMP)Wtsi
Genetic Background: involves: C57BL/6J * C57BL/6N

 MP:0003935 abnormal craniofacial development "anomaly in the process of forming the face and/or cranium" [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

 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: Spta1sph-3J/Spta1sph-3J
Genetic Background: NOD.Cg-H2b Spta1sph-3J

 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

 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

 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

 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

 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

 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

 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

 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

 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

 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

 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

 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

 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

 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

 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

 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

 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

 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

 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

 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

 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

 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

 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

 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

 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

 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

 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

 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"]
Show

Allelic Composition: Rdh10trex/Rdh10trex
Genetic Background: involves: 129S1/Sv * C57BL/6

 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"]
Show

Allelic Composition: Spta1sph-3J/Spta1sph-3J
Genetic Background: NOD.Cg-H2b Spta1sph-3J

Allelic Composition: Rdh10trex/Rdh10trex
Genetic Background: involves: 129S1/Sv * C57BL/6

 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"]
Show

Allelic Composition: Rdh10trex/Rdh10trex
Genetic Background: involves: 129S1/Sv * C57BL/6

 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

 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

 MP:0010940 abnormal maxillary prominence morphology 
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Allelic Composition: Spta1sph-3J/Spta1sph-3J
Genetic Background: NOD.Cg-H2b Spta1sph-3J

 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

 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

 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

 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

 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

 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

 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

 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

 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

 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

 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

 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

 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

 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]
Show

Allelic Composition: Spta1sph-3J/Spta1sph-3J
Genetic Background: NOD.Cg-H2b Spta1sph-3J

 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

 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

  


Interacting proteins (from Reactome)
Interactor ID Name Interaction type
 ENSMUSG00000039194 Rlbp1 / Q9Z275 / retinaldehyde binding protein 1 / P12271*  / reaction






 

1 s.

 
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