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Gene : DCAF17 Homo sapiens

Name  ? DDB1 and CUL4 associated factor 17 Cytological Location  2q31.1
Brief Description  DDB1 and CUL4 associated factor 17
Description  This gene encodes a nuclear transmembrane protein that associates with cullin 4A/damaged DNA binding protein 1 ubiquitin ligase complex. Mutations in this gene are associated with Woodhouse-Sakati syndrome. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Sep 2009]
  • synonyms:
  • C2orf37,
  • Woodhouse-Sakati syndrome,
  • OTTHUMG00000132259,
  • uc002ugx.3,
  • HGNC:25784,
  • chromosome 2 open reading frame 37,
  • FLJ13096,
  • AK023158,
  • DCAF17,
  • C20orf37,
  • NM_025000,
  • C2orf37
  • identifiers:
  • 80067,
  • ENSG00000115827,
  • DCAF17

Genome feature

Region: gene ? Length: 56864  
Location: 2:171434166-171491029 Cyto location: 2q31.1

Uni Prot Comments Displayer

Protein Atlas Displayer

Gene Expression Atlas Tissues Displayer

Gene Expression Atlas Diseases Displayer

Publication Counts Displayer

Curated Proteins Displayer


Gene Ontology Displayer

Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


J Browse Displayer

Gene Structure Displayer

Overlapping Features Displayer

Mouse Alleles Displayer

Gene --> Chromosomal location.

Gene --> GO terms.

Gene --> Overlapping genes.


Gene --> Proteins.


Gene Report --> GWAS hit


1 Diseases

Gene (Hum OR Rat) --> Mouse Allele (Phenotype)

Gene --> Alleles and Disease (clinVar data)

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


Homologue Displayer


Cytoscape Network Displayer

Gene --> Physical and Genetic Interactions


Gene(s) --> Significant SNPs (GTex data)

Gene Ontology

Gene --> GO terms.



732 SN Ps

5 Cross References

18 Data Sets

3 Homologues

0 Located Features

97 Rna Seq Results