WDR62 (WD repeat domain 62)

2014-02-01  

Identity

HGNC
LOCATION
19q13.12
LOCUSID
ALIAS
C19orf14,MCPH2
FUSION GENES

Other Information

Locus ID:

NCBI: 284403
MIM: 613583
HGNC: 24502
Ensembl: ENSG00000075702

Variants:

dbSNP: 284403
ClinVar: 284403
TCGA: ENSG00000075702
COSMIC: WDR62

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000075702ENST00000270301O43379
ENSG00000075702ENST00000401500O43379
ENSG00000075702ENST00000427823H7C3R4
ENSG00000075702ENST00000587391O43379
ENSG00000075702ENST00000644764A0A2R8YD43

Expression (GTEx)

0
50
100
150

Protein levels (Protein atlas)

Not detected
Low
Medium
High

References

Pubmed IDYearTitleCitations
389261762024Molecular genetics, neuroimaging outcomes, and structural analyses of novel and recurrent variants of WDR62 gene in two consanguineous Pakistani families with autosomal recessive primary microcephaly.0
389261762024Molecular genetics, neuroimaging outcomes, and structural analyses of novel and recurrent variants of WDR62 gene in two consanguineous Pakistani families with autosomal recessive primary microcephaly.0
357266082022Neurological outcome in WDR62 primary microcephaly.3
357582462022WD repeat domain 62 (WDR62) promotes resistance of colorectal cancer to oxaliplatin through modulating mitogen-activated protein kinase (MAPK) signaling.3
358088302022WDR62 variants contribute to congenital heart disease by inhibiting cardiomyocyte proliferation.4
357266082022Neurological outcome in WDR62 primary microcephaly.3
357582462022WD repeat domain 62 (WDR62) promotes resistance of colorectal cancer to oxaliplatin through modulating mitogen-activated protein kinase (MAPK) signaling.3
358088302022WDR62 variants contribute to congenital heart disease by inhibiting cardiomyocyte proliferation.4
339216532021Further Delineation of Phenotype and Genotype of Primary Microcephaly Syndrome with Cortical Malformations Associated with Mutations in the WDR62 Gene.3
341377882021WDR62 localizes katanin at spindle poles to ensure synchronous chromosome segregation.7
341377892021WDR62 regulates spindle dynamics as an adaptor protein between TPX2/Aurora A and katanin.13
343062582021Systematic Analysis of the Oncogenic Role of WDR62 in Human Tumors.5
343263222021An integrated functional and clinical genomics approach reveals genes driving aggressive metastatic prostate cancer.14
339216532021Further Delineation of Phenotype and Genotype of Primary Microcephaly Syndrome with Cortical Malformations Associated with Mutations in the WDR62 Gene.3
341377882021WDR62 localizes katanin at spindle poles to ensure synchronous chromosome segregation.7

Citation

Dessen P

WDR62 (WD repeat domain 62)

Atlas Genet Cytogenet Oncol Haematol. 2014-02-01

Online version: http://atlasgeneticsoncology.org/gene/53801/wdr62-(wd-repeat-domain-62)