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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Tbc1d32
TBC1 domain family, member 32
MGI:2442827
49 phenotypes from 6 alleles in 7 genetic backgrounds
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Allelic Composition
Genetic Background		 Annotated Term Reference
Tbc1d32b2b2284Clo/Tbc1d32b2b2284Clo
C57BL/6J-Tbc1d32b2b2284Clo 		abnormal aortic arch morphology J:175213
abnormal inferior vena cava morphology J:175213
anophthalmia J:175213
atrioventricular septal defect J:175213
cleft palate J:175213
cleft upper lip J:175213
dilated esophagus J:175213
double outlet right ventricle J:175213
facial cleft J:175213
heterotaxia J:175213
kidney cyst J:175213
left atrial isomerism J:175213
left pulmonary isomerism J:175213
mesocardia J:175213
persistent truncus arteriosus J:175213
polydactyly J:175213
preaxial polydactyly J:175213
premature closure of the ductus arteriosus J:175213
pulmonary artery hypoplasia J:175213
right aortic arch J:175213
right atrial isomerism J:175213
right-sided stomach J:175213
short snout J:175213
spleen hypoplasia J:175213
tracheoesophageal fistula J:175213
vascular ring J:175213
Tbc1d32b2b2596Clo/Tbc1d32b2b2596Clo
C57BL/6J-Tbc1d32b2b2596Clo 		abnormal frontonasal prominence morphology J:175213
anophthalmia J:175213
atrioventricular septal defect J:175213
cleft palate J:175213
cleft upper lip J:175213
dual inferior vena cava J:175213
duplex kidney J:175213
exencephaly J:175213
kidney cyst J:175213
microphthalmia J:175213
overriding aortic valve J:175213
persistent truncus arteriosus J:175213
persistent truncus arteriosus type i J:175213
polydactyly J:175213
pulmonary hypoplasia J:175213
right atrial isomerism J:175213
tracheoesophageal fistula J:175213
Tbc1d32b2b3260.1Clo/Tbc1d32b2b3260.1Clo
C57BL/6J-Tbc1d32b2b3260.1Clo 		abnormal kidney morphology J:175213
abnormal semilunar valve morphology J:175213
exencephaly J:175213
persistent truncus arteriosus J:175213
preaxial polydactyly J:175213
short snout J:175213
transposition of great arteries J:175213
Tbc1d32bromi/Tbc1d32bromi
involves: C57BL/6J 		abnormal embryonic neuroepithelium morphology J:158583
abnormal eye development J:158583
abnormal neural tube morphology J:158583
abnormal retina pigment epithelium morphology J:158583
exencephaly J:158583
preaxial polydactyly J:158583
retina hypoplasia J:158583
small lens J:158583
Tbc1d32bromi/Tbc1d32Gt(RRF165)Byg
involves: 129P2/OlaHsd * C3HeB/FeJ * C57BL/6J 		abnormal eye development J:158583
exencephaly J:158583
Tbc1d32em1(IMPC)J/Tbc1d32em1(IMPC)J
C57BL/6NJ-Tbc1d32em1(IMPC)J/Mmjax 		abnormal body wall morphology J:211773
abnormal embryo size J:211773
abnormal facial morphology J:211773
anophthalmia J:211773
cleft palate J:211773
edema J:211773
facial cleft J:211773
hemorrhage J:211773
polydactyly J:211773
preweaning lethality, complete penetrance J:211773
Tbc1d32Gt(RRF165)Byg/Tbc1d32Gt(RRF165)Byg
involves: 129P2/OlaHsd * C3HeB/FeJ 		abnormal eye development J:158583
exencephaly J:158583
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Send questions and comments to User Support. 		last database update
04/16/2024
MGI 6.23 		The Jackson Laboratory