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KCNE2

KCNE2
Available structures
PDB Ortholog search: PDBe RCSB
Identifiers
Aliases KCNE2, ATFB4, LQT5, LQT6, MIRP1, potassium voltage-gated channel subfamily E regulatory subunit 2
External IDs OMIM: 603796 MGI: 1891123 HomoloGene: 71688 GeneCards: KCNE2
Orthologs
Species Human Mouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_172201

NM_134110

RefSeq (protein)

NP_751951

NP_598871.1
NP_598871

Location (UCSC) Chr 21: 34.36 – 34.37 Mb Chr 16: 92.29 – 92.3 Mb
PubMed search

2M0Q

NM_172201

NM_134110

NP_751951

NP_598871.1
NP_598871

Potassium voltage-gated channel subfamily E member 2 (KCNE2), also known as MinK-related peptide 1 (MiRP1), is a protein that in humans is encoded by the KCNE2 gene on chromosome 21. MiRP1 is a voltage-gated potassium channel accessory subunit (beta subunit) associated with Long QT syndrome. It is ubiquitously expressed in many tissues and cell types. Because of this and its ability to regulate multiple different ion channels, KCNE2 exerts considerable influence on a number of cell types and tissues. Human KCNE2 is a member of the five-strong family of human KCNE genes. KCNE proteins contain a single membrane-spanning region, extracellular N-terminal and intracellular C-terminal. KCNE proteins have been widely studied for their roles in the heart and in genetic predisposition to inherited cardiac arrhythmias. The KCNE2 gene also contains one of 27 SNPs associated with increased risk of coronary artery disease. More recently, roles for KCNE proteins in a variety of non-cardiac tissues have also been explored.


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