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Name
ID

Crb2
crumbs family member 2
MGI:2679260

Phenotype annotations related to cardiovascular system

Darker colors indicate more annotations

Human Phenotypes	Fetal pericardial effusion	Ventricular septal defect	Vascular dilatation
Disease(s) Associated with CRB2
ventriculomegaly - cystic kidney disease

Mouse Phenotypes		abnormal retina blood vessel morphology	retina neovascularization	abnormal vitelline vasculature morphology	absent heart tube
Availability	Mouse Genotype	abnormal retina blood vessel morphology	retina neovascularization	abnormal vitelline vasculature morphology	absent heart tube
	Crb2^tm1Vlcg/Crb2^tm1Vlcg
	Crb2^tm1.1Wij/Crb2^tm1.1Wij Tg(Chx10-EGFP/cre,-ALPP)2Clc/0 (conditional)
	Crb2^tm1.1Wij/Crb2^tm1.1Wij Tg(Crx-cre)1Tfur/0 (conditional)

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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