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Symbol Name ID |
Ube2a
ubiquitin-conjugating enzyme E2A MGI:102959 |
| Darker colors indicate more annotations |
| Human Phenotypes | Neonatal hyperbilirubinemia |
| Disease(s) Associated with UBE2A | |
| syndromic X-linked intellectual disability Nascimento type |
| Mouse Phenotypes | decreased circulating serum albumin level |
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| Availability | Mouse Genotype | |
| Ube2atm1.1(KOMP)Vlcg/Ube2atm1.1(KOMP)Vlcg | ||
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 08/02/2024 MGI 6.24 |
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