DCAF17
Identifiers
AliasesDCAF17, C2orf37, DDB1 and CUL4 associated factor 17, C20orf37
External IDsOMIM: 612515 MGI: 1923013 HomoloGene: 65979 GeneCards: DCAF17
Orthologs
SpeciesHumanMouse
Entrez

80067

75763

Ensembl

ENSG00000115827

ENSMUSG00000041966

UniProt

Q5H9S7

Q3TUL7

RefSeq (mRNA)

NM_001164821
NM_025000

NM_001165980
NM_001165981
NM_001165982
NM_198005

RefSeq (protein)

NP_001158293
NP_079276

NP_001159452
NP_001159453
NP_001159454
NP_932122

Location (UCSC)Chr 2: 171.43 – 171.49 MbChr 2: 71.06 – 71.1 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

DDB1 and CUL4 associated factor 17 is a protein that in humans is encoded buy the DCAF17 gene.[5]

Function

DCAF17 is a nuclear transmembrane protein that associates with cullin 4A / damaged DNA binding protein 1 ubiquitin ligase complex.[5]

Clinical significance

Mutations in this gene are associated with Woodhouse–Sakati syndrome.[5]

References

  1. 1 2 3 GRCh38: Ensembl release 89: ENSG00000115827 - Ensembl, May 2017
  2. 1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000041966 - Ensembl, May 2017
  3. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. 1 2 3 "Entrez Gene: DDB1 and CUL4 associated factor 17".

Further reading

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