ZNF592 Chromosome 15
Zinc finger protein 592
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What This Gene Does
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]
Gene Info
Gene Group
Zinc fingers C2H2-type
Locus Type
gene with protein product
Location
15q25.3
Ensembl
ENSG00000166716
All Variants (1)
| RSID | Category | Clinical Significance | Conditions |
|---|---|---|---|
| RS145206161 | Health Risk | Conflicting classifications of pathogenicity | — |