Entity Details

Primary name DCAF17
Entity type gene
Source Source Link

Details

PrimaryID80067
RefseqGeneNG_013038
SymbolDCAF17
NameDDB1 and CUL4 associated factor 17
Chromosome2
Location2q31.1
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate2001-03-12
ModificationDate2021-06-11

Ontological Relatives

UniProt IDsDCA17_HUMAN

GO terms

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GOName
GO:0005654 nucleoplasm
GO:0005730 nucleolus
GO:0005829 cytosol
GO:0016021 integral component of membrane
GO:0016567 protein ubiquitination
GO:0043687 post-translational protein modification
GO:0080008 Cul4-RING E3 ubiquitin ligase complex

Diseases

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Disease IDSourceNameDescription
241080 OMIMWoodhouse-Sakati syndrome (WDSKS)A rare autosomal recessive disorder characterized by hypogonadism, alopecia, diabetes mellitus, mental retardation, and extrapyramidal syndrome. The disease is caused by variants affecting the gene represented in this entry.

Interactions

8 interactions