Identity
HGNC
LOCATION
21q22.11
LOCUSID
ALIAS
ATFB4,LQT5,LQT6,MIRP1
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: 9992
MIM: 603796
HGNC: 6242
Ensembl: ENSG00000159197
Variants:
dbSNP: 9992
ClinVar: 9992
TCGA: ENSG00000159197
COSMIC: KCNE2
RNA/Proteins
| Gene ID | Transcript ID | Uniprot |
|---|---|---|
| ENSG00000159197 | ENST00000290310 | Q9Y6J6 |
Expression (GTEx)
Pathways
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 31044566 | 2019 | miR-584-5p regulates hepatocellular carcinoma cell migration and invasion through targeting KCNE2. | 11 |
| 31270966 | 2019 | The research of ion channel-related gene polymorphisms with atrial fibrillation in the Chinese Han population. | 3 |
| 31679457 | 2019 | A conserved arginine/lysine-based motif promotes ER export of KCNE1 and KCNE2 to regulate KCNQ1 channel activity. | 4 |
| 31044566 | 2019 | miR-584-5p regulates hepatocellular carcinoma cell migration and invasion through targeting KCNE2. | 11 |
| 31270966 | 2019 | The research of ion channel-related gene polymorphisms with atrial fibrillation in the Chinese Han population. | 3 |
| 31679457 | 2019 | A conserved arginine/lysine-based motif promotes ER export of KCNE1 and KCNE2 to regulate KCNQ1 channel activity. | 4 |
| 28280005 | 2017 | Kcne2 deletion impairs insulin secretion and causes type 2 diabetes mellitus. | 18 |
| 28794082 | 2017 | Loss-of-Function KCNE2 Variants: True Monogenic Culprits of Long-QT Syndrome or Proarrhythmic Variants Requiring Secondary Provocation? | 15 |
| 28280005 | 2017 | Kcne2 deletion impairs insulin secretion and causes type 2 diabetes mellitus. | 18 |
| 28794082 | 2017 | Loss-of-Function KCNE2 Variants: True Monogenic Culprits of Long-QT Syndrome or Proarrhythmic Variants Requiring Secondary Provocation? | 15 |
| 26956495 | 2016 | Filamin C: a novel component of the KCNE2 interactome during hypoxia. | 3 |
| 26956495 | 2016 | Filamin C: a novel component of the KCNE2 interactome during hypoxia. | 3 |
| 26123744 | 2015 | The KCNE2 K⁺ channel regulatory subunit: Ubiquitous influence, complex pathobiology. | 34 |
| 26123744 | 2015 | The KCNE2 K⁺ channel regulatory subunit: Ubiquitous influence, complex pathobiology. | 34 |
| 24460807 | 2014 | Single nucleotide polymorphisms in proximity to K-channel genes are associated with decreased longitudinal QTc variance. | 1 |
Citation
Dessen P
KCNE2 (potassium voltage-gated channel subfamily E regulatory subunit 2)
Atlas Genet Cytogenet Oncol Haematol. 2011-01-01
Online version: http://atlasgeneticsoncology.org/gene/51948/kcne2
