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Symbol Name ID |
Ndn
necdin, MAGE family member MGI:97290 |
| Darker colors indicate more annotations |
| Human Phenotypes | Gastroparesis |
Hypotonia |
Generalized hypotonia |
Neonatal hypotonia |
Decreased muscle mass |
| Disease(s) Associated with NDN | |||||
| Prader-Willi syndrome |
| Mouse Phenotypes | hypotonia |
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| Availability | Mouse Genotype | |
| Ndntm1Stw/Ndn+ | ||
| Ndntm2Stw/Ndn+ | ||
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 04/16/2024 MGI 6.23 |
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