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: 79734
MIM: 616386
HGNC: 25705
Ensembl: ENSG00000100379
Variants:
dbSNP: 79734
ClinVar: 79734
TCGA: ENSG00000100379
COSMIC: KCTD17
RNA/Proteins
Expression (GTEx)
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 25983243 | 2015 | A missense mutation in KCTD17 causes autosomal dominant myoclonus-dystonia. | 45 |
| 25983243 | 2015 | A missense mutation in KCTD17 causes autosomal dominant myoclonus-dystonia. | 45 |
Citation
Dessen P
KCTD17 (potassium channel tetramerization domain containing 17)
Atlas Genet Cytogenet Oncol Haematol. 2014-11-01
Online version: http://atlasgeneticsoncology.org/gene/64822/kctd17-(potassium-channel-tetramerization-domain-containing-17)
