ZNF592 a probable transcriptional regulator. Belongs to the krueppel C2H2-type zinc-finger protein family. Widely expressed, with highest levels in skeletal muscle. Expressed throughout the central nervous system, including in the cerebellum and cerebellar vermis, with higher expression in the substantia nigra. Widely expressed in fetal tissues. Note: This description may include information from UniProtKB.
Protein type: C2H2-type zinc finger protein
Chromosomal Location of human Ortholog: 15q25.3
Cellular Component:  nucleus
Molecular Function:  DNA binding; DNA-binding transcription factor activity, RNA polymerase II-specific; metal ion binding; protein binding
Biological Process:  regulation of transcription by RNA polymerase II
Disease: Galloway-mowat Syndrome
Reference #:  Q92610 (UniProtKB)
Alt. Names/Synonyms: CAMOS; KIAA0211; MGC138437; MGC138439; SCAR5; Zinc finger protein 592; ZN592; ZNF592
Gene Symbols: ZNF592
Molecular weight: 137,528 Da
Basal Isoelectric point: 8.1  Predict pI for various phosphorylation states
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ZNF592

Protein Structure Not Found.

Cross-references to other databases:  AlphaFold  |  STRING  |  cBioPortal  |  Wikipedia  |  neXtProt  |  Protein Atlas  |  BioGPS  |  Pfam  |  Phospho.ELM  |  NetworKIN  |  UniProtKB  |  Entrez-Gene  |  GenPept  |  Ensembl Gene