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: 23630
MIM: 300328
HGNC: 6241
Ensembl: ENSG00000176076
Variants:
dbSNP: 23630
ClinVar: 23630
TCGA: ENSG00000176076
COSMIC: KCNE5
RNA/Proteins
| Gene ID | Transcript ID | Uniprot |
|---|---|---|
| ENSG00000176076 | ENST00000372101 | Q9UJ90 |
Expression (GTEx)
Pathways
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 30129429 | 2018 | Case report of familial sudden cardiac death caused by a DSG2 p.F531C mutation as genetic background when carrying with heterozygous KCNE5 p.D92E/E93X mutation. | 6 |
| 30129429 | 2018 | Case report of familial sudden cardiac death caused by a DSG2 p.F531C mutation as genetic background when carrying with heterozygous KCNE5 p.D92E/E93X mutation. | 6 |
| 21985337 | 2012 | KCNE5 polymorphism rs697829 is associated with QT interval and survival in acute coronary syndromes patients. | 7 |
| 21985337 | 2012 | KCNE5 polymorphism rs697829 is associated with QT interval and survival in acute coronary syndromes patients. | 7 |
| 21493962 | 2011 | KCNE5 (KCNE1L) variants are novel modulators of Brugada syndrome and idiopathic ventricular fibrillation. | 55 |
| 21730298 | 2011 | Novel expression and regulation of voltage-dependent potassium channels in placentas from women with preeclampsia. | 23 |
| 21493962 | 2011 | KCNE5 (KCNE1L) variants are novel modulators of Brugada syndrome and idiopathic ventricular fibrillation. | 55 |
| 21730298 | 2011 | Novel expression and regulation of voltage-dependent potassium channels in placentas from women with preeclampsia. | 23 |
| 18313602 | 2008 | Gain of function in IKs secondary to a mutation in KCNE5 associated with atrial fibrillation. | 45 |
| 18313602 | 2008 | Gain of function in IKs secondary to a mutation in KCNE5 associated with atrial fibrillation. | 45 |
| 18313602 | 2008 | Gain of function in IKs secondary to a mutation in KCNE5 associated with atrial fibrillation. | 45 |
| 18313602 | 2008 | Gain of function in IKs secondary to a mutation in KCNE5 associated with atrial fibrillation. | 45 |
| 16054468 | 2005 | Relation of 97T polymorphism in KCNE5 to risk of atrial fibrillation. | 23 |
| 16054468 | 2005 | Relation of 97T polymorphism in KCNE5 to risk of atrial fibrillation. | 23 |
| 15193977 | 2004 | Does KCNE5 play a role in long QT syndrome? | 6 |
Citation
Dessen P
KCNE5 (potassium voltage-gated channel subfamily E regulatory subunit 5)
Atlas Genet Cytogenet Oncol Haematol. 2015-06-01
Online version: http://atlasgeneticsoncology.org/gene/77664/kcne5-(potassium-voltage-gated-channel-subfamily-e-regulatory-subunit-5)
