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: 80067
MIM: 612515
HGNC: 25784
Ensembl: ENSG00000115827
Variants:
dbSNP: 80067
ClinVar: 80067
TCGA: ENSG00000115827
COSMIC: DCAF17
RNA/Proteins
Expression (GTEx)
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 34877714 | 2022 | Novel splicing-site mutation in DCAF17 gene causing Woodhouse-Sakati syndrome in a large consanguineous family. | 3 |
| 34877714 | 2022 | Novel splicing-site mutation in DCAF17 gene causing Woodhouse-Sakati syndrome in a large consanguineous family. | 3 |
| 34732557 | 2021 | Woodhouse-Sakati syndrome (WSS): A case report of 3 Saudi sisters with urogenital anomalies. | 4 |
| 34732557 | 2021 | Woodhouse-Sakati syndrome (WSS): A case report of 3 Saudi sisters with urogenital anomalies. | 4 |
| 31323129 | 2020 | Woodhouse-Sakati syndrome in a family is associated with a homozygous start loss mutation in the DCAF17 gene. | 4 |
| 31323129 | 2020 | Woodhouse-Sakati syndrome in a family is associated with a homozygous start loss mutation in the DCAF17 gene. | 4 |
| 29178422 | 2018 | Novel inactivating mutations of the DCAF17 gene in American and Turkish families cause male infertility and female subfertility in the mouse model. | 8 |
| 29574468 | 2018 | Phenotypic Variability of c.436delC DCAF17 Gene Mutation in Woodhouse-Sakati Syndrome. | 5 |
| 29178422 | 2018 | Novel inactivating mutations of the DCAF17 gene in American and Turkish families cause male infertility and female subfertility in the mouse model. | 8 |
| 29574468 | 2018 | Phenotypic Variability of c.436delC DCAF17 Gene Mutation in Woodhouse-Sakati Syndrome. | 5 |
| 26612766 | 2016 | Exome sequencing revealed a novel biallelic deletion in the DCAF17 gene underlying Woodhouse Sakati syndrome. | 10 |
| 26612766 | 2016 | Exome sequencing revealed a novel biallelic deletion in the DCAF17 gene underlying Woodhouse Sakati syndrome. | 10 |
| 26440089 | 2015 | Novel compound heterozygous frameshift mutations of C2orf37 in a familial Indian case of Woodhouse-Sakati syndrome. | 3 |
| 26440089 | 2015 | Novel compound heterozygous frameshift mutations of C2orf37 in a familial Indian case of Woodhouse-Sakati syndrome. | 3 |
| 24015686 | 2014 | Alopecia and hypotrichosis as characteristic findings in Woodhouse-Sakati syndrome: report of a family with mutation in the C2orf37 gene. | 3 |
Citation
Dessen P
DCAF17 (DDB1 and CUL4 associated factor 17)
Atlas Genet Cytogenet Oncol Haematol. 2014-11-01
Online version: http://atlasgeneticsoncology.org/gene/62317/dcaf17-(ddb1-and-cul4-associated-factor-17)
