Symbol Name ID |
Wdr19
WD repeat domain 19 MGI:2443231 |
Darker colors indicate more annotations |
Human Phenotypes | Photophobia |
Aplasia/Hypoplasia of the cerebellar vermis |
Ataxia |
Polydipsia |
Intellectual disability |
Intellectual disability, mild |
Hyperreflexia |
Global developmental delay |
Disease(s) Associated with WDR19 | ||||||||
retinitis pigmentosa | ||||||||
Senior-Loken syndrome |
Mouse Phenotypes | exencephaly |
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Availability | Mouse Genotype | |
Wdr19twto/Wdr19twto |
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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