Identity
HGNC
LOCATION
1q42.11
LOCUSID
ALIAS
CDW2,GID7,MIP2,SKDEAS
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: 80232
MIM: 617424
HGNC: 21208
Ensembl: ENSG00000162923
Variants:
dbSNP: 80232
ClinVar: 80232
TCGA: ENSG00000162923
COSMIC: WDR26
RNA/Proteins
Expression (GTEx)
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 38575527 | 2024 | Skraban-Deardorff intellectual disability syndrome-associated mutations in WDR26 impair CTLH E3 complex assembly. | 1 |
| 38575527 | 2024 | Skraban-Deardorff intellectual disability syndrome-associated mutations in WDR26 impair CTLH E3 complex assembly. | 1 |
| 35627197 | 2022 | Two Novel Variants of WDR26 in Chinese Patients with Intellectual Disability. | 0 |
| 35627197 | 2022 | Two Novel Variants of WDR26 in Chinese Patients with Intellectual Disability. | 0 |
| 33506510 | 2021 | Skraban-Deardorff syndrome: Six new cases of WDR26-related disease and expansion of the clinical phenotype. | 2 |
| 33675273 | 2021 | Expanding the clinical phenotype of the ultra-rare Skraban-Deardorff syndrome: Two novel individuals with WDR26 loss-of-function variants and a literature review. | 2 |
| 33905682 | 2021 | GID E3 ligase supramolecular chelate assembly configures multipronged ubiquitin targeting of an oligomeric metabolic enzyme. | 27 |
| 33506510 | 2021 | Skraban-Deardorff syndrome: Six new cases of WDR26-related disease and expansion of the clinical phenotype. | 2 |
| 33675273 | 2021 | Expanding the clinical phenotype of the ultra-rare Skraban-Deardorff syndrome: Two novel individuals with WDR26 loss-of-function variants and a literature review. | 2 |
| 33905682 | 2021 | GID E3 ligase supramolecular chelate assembly configures multipronged ubiquitin targeting of an oligomeric metabolic enzyme. | 27 |
| 32958140 | 2020 | WD40 Repeat Protein 26 Negatively Regulates Formyl Peptide Receptor-1 Mediated Wound Healing in Intestinal Epithelial Cells. | 1 |
| 32958140 | 2020 | WD40 Repeat Protein 26 Negatively Regulates Formyl Peptide Receptor-1 Mediated Wound Healing in Intestinal Epithelial Cells. | 1 |
| 28686853 | 2017 | WDR26 Haploinsufficiency Causes a Recognizable Syndrome of Intellectual Disability, Seizures, Abnormal Gait, and Distinctive Facial Features. | 20 |
| 28686853 | 2017 | WDR26 Haploinsufficiency Causes a Recognizable Syndrome of Intellectual Disability, Seizures, Abnormal Gait, and Distinctive Facial Features. | 20 |
| 26895380 | 2016 | Upregulated WDR26 serves as a scaffold to coordinate PI3K/ AKT pathway-driven breast cancer cell growth, migration, and invasion. | 30 |
Citation
Dessen P
WDR26 (WD repeat domain 26)
Atlas Genet Cytogenet Oncol Haematol. 2013-09-01
Online version: http://atlasgeneticsoncology.org/gene/53496/wdr26-(wd-repeat-domain-26)
