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: 22884
MIM: 618586
HGNC: 31406
Ensembl: ENSG00000047056
Variants:
dbSNP: 22884
ClinVar: 22884
TCGA: ENSG00000047056
COSMIC: WDR37
RNA/Proteins
Expression (GTEx)
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 36683218 | 2023 | Chemotherapy-Induced Senescence Reprogramming Promotes Nasopharyngeal Carcinoma Metastasis by circRNA-Mediated PKR Activation. | 5 |
| 36683218 | 2023 | Chemotherapy-Induced Senescence Reprogramming Promotes Nasopharyngeal Carcinoma Metastasis by circRNA-Mediated PKR Activation. | 5 |
| 33369122 | 2021 | Coloboma may be a shared feature in a spectrum of disorders caused by mutations in the WDR37-PACS1-PACS2 axis. | 7 |
| 33369122 | 2021 | Coloboma may be a shared feature in a spectrum of disorders caused by mutations in the WDR37-PACS1-PACS2 axis. | 7 |
| 32530092 | 2020 | Expanding the phenotypic spectrum consequent upon de novo WDR37 missense variants. | 4 |
| 32530092 | 2020 | Expanding the phenotypic spectrum consequent upon de novo WDR37 missense variants. | 4 |
| 31327508 | 2019 | De Novo Variants in WDR37 Are Associated with Epilepsy, Colobomas, Dysmorphism, Developmental Delay, Intellectual Disability, and Cerebellar Hypoplasia. | 24 |
| 31327510 | 2019 | De Novo Missense Variants in WDR37 Cause a Severe Multisystemic Syndrome. | 17 |
| 31327508 | 2019 | De Novo Variants in WDR37 Are Associated with Epilepsy, Colobomas, Dysmorphism, Developmental Delay, Intellectual Disability, and Cerebellar Hypoplasia. | 24 |
| 31327510 | 2019 | De Novo Missense Variants in WDR37 Cause a Severe Multisystemic Syndrome. | 17 |
| 19851296 | 2010 | Assessment of a polymorphism of SDK1 with hypertension in Japanese Individuals. | 7 |
| 20198315 | 2010 | Association of genetic variants with hemorrhagic stroke in Japanese individuals. | 17 |
| 20379614 | 2010 | Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score. | 78 |
| 20383146 | 2010 | New loci associated with kidney function and chronic kidney disease. | 433 |
| 20677014 | 2010 | An approach based on a genome-wide association study reveals candidate loci for narcolepsy. | 19 |
Citation
Dessen P
WDR37 (WD repeat domain 37)
Atlas Genet Cytogenet Oncol Haematol. 2014-11-01
Online version: http://atlasgeneticsoncology.org/gene/75710/wdr37-(wd-repeat-domain-37)
