|
Symbol Name ID |
Tubgcp2
tubulin, gamma complex component 2 MGI:1921487 |
| Darker colors indicate more annotations |
| Human Phenotypes | Optic atrophy |
Cerebral visual impairment |
| Disease(s) Associated with TUBGCP2 | ||
| pachygyria, microcephaly, developmental delay, and dysmorphic facies, with or without seizures |
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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