WDR26 (WD repeat domain 26)

2013-09-01  

Identity

HGNC
LOCATION
1q42.11
LOCUSID
ALIAS
CDW2,GID7,MIP2,SKDEAS
FUSION GENES

Other Information

Locus ID:

NCBI: 80232
MIM: 617424
HGNC: 21208
Ensembl: ENSG00000162923

Variants:

dbSNP: 80232
ClinVar: 80232
TCGA: ENSG00000162923
COSMIC: WDR26

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000162923ENST00000414423A0A499FIZ0
ENSG00000162923ENST00000445239C9JCS7
ENSG00000162923ENST00000480676H0Y9R3
ENSG00000162923ENST00000486652H0Y917
ENSG00000162923ENST00000651911Q9H7D7

Expression (GTEx)

0
10
20
30
40
50
60
70
80

Protein levels (Protein atlas)

Not detected
Low
Medium
High

References

Pubmed IDYearTitleCitations
259189942015Genome-wide methylation study on depression: differential methylation and variable methylation in monozygotic twins.21
153786032004WDR26: a novel Gbeta-like protein, suppresses MAPK signaling pathway.14
268953802016Upregulated WDR26 serves as a scaffold to coordinate PI3K/ AKT pathway-driven breast cancer cell growth, migration, and invasion.14
220655752011The WD40 repeat protein WDR26 binds Gβγ and promotes Gβγ-dependent signal transduction and leukocyte migration.13
194466062009A novel WD-40 repeat protein WDR26 suppresses H2O2-induced cell death in neural cells.10
236259272013WDR26 functions as a scaffolding protein to promote Gβγ-mediated phospholipase C β2 (PLCβ2) activation in leukocytes.8
270984532016WDR26 is a new partner of Axin1 in the canonical Wnt signaling pathway.8
286868532017WDR26 Haploinsufficiency Causes a Recognizable Syndrome of Intellectual Disability, Seizures, Abnormal Gait, and Distinctive Facial Features.8
201711912010Overexpression of MIP2, a novel WD-repeat protein, promotes proliferation of H9c2 cells.6
278356842016Characterization of Novel Molecular Mechanisms Favoring Rac1 Membrane Translocation.1

Citation

Dessen P

WDR26 (WD repeat domain 26)

Atlas Genet Cytogenet Oncol Haematol. 2013-09-01

Online version: http://atlasgeneticsoncology.org/gene/53496/wdr26