Identity
HGNC
LOCATION
19q13.12
LOCUSID
ALIAS
C19orf14,MCPH2
FUSION GENES
Non-annotated gene. Preliminary data : if you are an author who wish to write a full paper/card on this gene, contribute in submission tool
Other Information
Locus ID:
NCBI: 284403
MIM: 613583
HGNC: 24502
Ensembl: ENSG00000075702
Variants:
dbSNP: 284403
ClinVar: 284403
TCGA: ENSG00000075702
COSMIC: WDR62
RNA/Proteins
Expression (GTEx)
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 38926176 | 2024 | Molecular 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 |
| 38926176 | 2024 | Molecular 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 |
| 35726608 | 2022 | Neurological outcome in WDR62 primary microcephaly. | 3 |
| 35758246 | 2022 | WD repeat domain 62 (WDR62) promotes resistance of colorectal cancer to oxaliplatin through modulating mitogen-activated protein kinase (MAPK) signaling. | 3 |
| 35808830 | 2022 | WDR62 variants contribute to congenital heart disease by inhibiting cardiomyocyte proliferation. | 4 |
| 35726608 | 2022 | Neurological outcome in WDR62 primary microcephaly. | 3 |
| 35758246 | 2022 | WD repeat domain 62 (WDR62) promotes resistance of colorectal cancer to oxaliplatin through modulating mitogen-activated protein kinase (MAPK) signaling. | 3 |
| 35808830 | 2022 | WDR62 variants contribute to congenital heart disease by inhibiting cardiomyocyte proliferation. | 4 |
| 33921653 | 2021 | Further Delineation of Phenotype and Genotype of Primary Microcephaly Syndrome with Cortical Malformations Associated with Mutations in the WDR62 Gene. | 3 |
| 34137788 | 2021 | WDR62 localizes katanin at spindle poles to ensure synchronous chromosome segregation. | 7 |
| 34137789 | 2021 | WDR62 regulates spindle dynamics as an adaptor protein between TPX2/Aurora A and katanin. | 13 |
| 34306258 | 2021 | Systematic Analysis of the Oncogenic Role of WDR62 in Human Tumors. | 5 |
| 34326322 | 2021 | An integrated functional and clinical genomics approach reveals genes driving aggressive metastatic prostate cancer. | 14 |
| 33921653 | 2021 | Further Delineation of Phenotype and Genotype of Primary Microcephaly Syndrome with Cortical Malformations Associated with Mutations in the WDR62 Gene. | 3 |
| 34137788 | 2021 | WDR62 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)
