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Symbol
Name
ID

Sh3pxd2b
SH3 and PX domains 2B
MGI:2442062

Phenotype annotations related to cardiovascular system

Darker colors indicate more annotations

Human Phenotypes	Atrial septal defect	Patent foramen ovale	Secundum atrial septal defect	Ventricular septal defect	Double outlet right ventricle	Mitral valve prolapse
Disease(s) Associated with SH3PXD2B
Frank-Ter Haar syndrome

Mouse Phenotypes		abnormal myocardial trabeculae morphology	abnormal mitral valve morphology	mitral valve prolapse	thin interventricular septum	abnormal heart shape	abnormal heart ventricle morphology	hyphema	decreased heart rate	corneal vascularization
Availability	Mouse Genotype	abnormal myocardial trabeculae morphology	abnormal mitral valve morphology	mitral valve prolapse	thin interventricular septum	abnormal heart shape	abnormal heart ventricle morphology	hyphema	decreased heart rate	corneal vascularization
	Sh3pxd2b^{Gt(GST_1527_E5)Lex}/Sh3pxd2b^{Gt(GST_1527_E5)Lex}
	Sh3pxd2b^nee/Sh3pxd2b^nee

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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