Tbc1d32 Phenotype Annotations

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

Allelic Composition Genetic Background	Annotated Term	Reference
Tbc1d32^b2b2284Clo/Tbc1d32^b2b2284Clo C57BL/6J-Tbc1d32^b2b2284Clo	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
Tbc1d32^b2b2596Clo/Tbc1d32^b2b2596Clo C57BL/6J-Tbc1d32^b2b2596Clo	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
Tbc1d32^b2b3260.1Clo/Tbc1d32^b2b3260.1Clo C57BL/6J-Tbc1d32^b2b3260.1Clo	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
Tbc1d32^bromi/Tbc1d32^bromi 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
Tbc1d32^bromi/Tbc1d32^{Gt(RRF165)Byg} involves: 129P2/OlaHsd * C3HeB/FeJ * C57BL/6J	abnormal eye development	J:158583
	exencephaly	J:158583
Tbc1d32^em1(IMPC)J/Tbc1d32^em1(IMPC)J C57BL/6NJ-Tbc1d32^em1(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
Tbc1d32^{Gt(RRF165)Byg}/Tbc1d32^{Gt(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)
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support.	last database update 11/12/2024 MGI 6.24