Symbol Name ID |
Sh3pxd2b
SH3 and PX domains 2B MGI:2442062 |
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 |
cornea vascularization |
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Availability | Mouse Genotype | |||||||||
Sh3pxd2bGt(GST_1527_E5)Lex/Sh3pxd2bGt(GST_1527_E5)Lex | ||||||||||
Sh3pxd2bnee/Sh3pxd2bnee |
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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last database update 09/03/2024 MGI 6.24 |
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