WDR4 (WD repeat domain 4)

2017-10-01  

Identity

HGNC
LOCATION
21q22.3
LOCUSID
ALIAS
GAMOS6,MIGSB,TRM82,TRMT82,Wuho,hWH
FUSION GENES

Other Information

Locus ID:

NCBI: 10785
MIM: 605924
HGNC: 12756
Ensembl: ENSG00000160193

Variants:

dbSNP: 10785
ClinVar: 10785
TCGA: ENSG00000160193
COSMIC: WDR4

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000160193ENST00000330317P57081
ENSG00000160193ENST00000398208P57081

Expression (GTEx)

0
5
10
15
20
25

Pathways

PathwaySourceExternal ID
Gene ExpressionREACTOMER-HSA-74160
tRNA processingREACTOMER-HSA-72306
tRNA modification in the nucleus and cytosolREACTOMER-HSA-6782315

Protein levels (Protein atlas)

Not detected
Low
Medium
High

References

Pubmed IDYearTitleCitations
264160262015Mutation in WDR4 impairs tRNA m(7)G46 methylation and causes a distinct form of microcephalic primordial dwarfism.24
286919272017Ubiquitination of tumor suppressor PML regulates prometastatic and immunosuppressive tumor microenvironment.9
267510692016Wuho Is a New Member in Maintaining Genome Stability through its Interaction with Flap Endonuclease 1.5
286179652018Further delineation of the phenotype caused by biallelic variants in the WDR4 gene.5
300794902018Mutations in WDR4 as a new cause of Galloway-Mowat syndrome.2

Citation

Dessen P

WDR4 (WD repeat domain 4)

Atlas Genet Cytogenet Oncol Haematol. 2017-10-01

Online version: http://atlasgeneticsoncology.org/gene/57078/wdr4