ZNF592 gene

zinc finger protein 592

The information on this page was automatically extracted from online scientific databases.

From NCBI Gene:

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]

From UniProt:

May be involved in transcriptional regulation.

Cytogenetic Location: 15q25.3, which is the long (q) arm of chromosome 15 at position 25.3

Molecular Location: base pairs 84,748,556 to 84,806,432 on chromosome 15 (Homo sapiens Annotation Release 108, GRCh38.p7) (NCBI)

Cytogenetic Location: 15q25.3, which is the long (q) arm of chromosome 15 at position 25.3
  • CAMOS
  • SCAR5