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Symbol Name ID |
Wnt5a
wingless-type MMTV integration site family, member 5A MGI:98958 |
| Darker colors indicate more annotations |
| Human Phenotypes | Right ventricular outlet tract obstruction |
| Disease(s) Associated with WNT5A | |
| autosomal dominant Robinow syndrome 1 |
| Mouse Phenotypes | pulmonary artery hypoplasia |
persistent truncus arteriosus |
double outlet right ventricle |
atrioventricular septal defect |
heart left ventricle hypoplasia |
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| Availability | Mouse Genotype | |||||
| Wnt5ab2b3077.1Clo/Wnt5ab2b3077.1Clo | ||||||
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 04/30/2024 MGI 6.23 |
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