|
Symbol Name ID |
Kmt5b
lysine methyltransferase 5B MGI:2444557 |
| Darker colors indicate more annotations |
| Human Phenotypes | Sparse lateral eyebrow |
| Disease(s) Associated with KMT5B | |
| autosomal dominant intellectual developmental disorder 51 |
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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