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Symbol Name ID |
Wdr19
WD repeat domain 19 MGI:2443231 |
| Darker colors indicate more annotations |
| Human Phenotypes | Neonatal hypotonia |
| Disease(s) Associated with WDR19 | |
| cranioectodermal dysplasia 4 |
| Mouse Phenotypes | abnormal myotome development |
abnormal dermomyotome development |
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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 04/16/2024 MGI 6.23 |
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