| Gene Symbol | ZNF592 |
| Entrez Gene ID | 9640 |
| Full Name | zinc finger protein 592 |
| Synonyms | CAMOS,SCAR5 |
| General protein information |
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| Gene Type | protein-coding |
| Organism | Homo sapiens(Human) |
| Genome | |
| Summary | This gene is thought to play a role in a complex developmental pathway and the regulation of genes involved in cerebellar development. Mutations in this gene have been associated with autosomal recessive spinocerebellar ataxia. [provided by RefSeq, Jan 2011]. |
| Disorder MIM: |









































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