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Symbol Name ID |
Sprtn
SprT-like N-terminal domain MGI:2685351 |
| Darker colors indicate more annotations |
| Human Phenotypes | Lipodystrophy |
| Disease(s) Associated with SPRTN | |
| Ruijs-Aalfs syndrome |
| Mouse Phenotypes | decreased white fat cell size |
decreased gonadal fat pad weight |
decreased inguinal fat pad weight |
decreased renal fat pad weight |
decreased interscapular fat pad weight |
decreased total fat pad weight |
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| Availability | Mouse Genotype | ||||||
| Sprtntm1Yjm/Sprtntm1Yjm | |||||||
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 05/07/2024 MGI 6.23 |
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