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KCNH5

KCNH5
Identifiers
Aliases KCNH5, EAG2, H-EAG2, Kv10.2, hEAG2, potassium voltage-gated channel subfamily H member 5
External IDs MGI: 3584508 HomoloGene: 15858 GeneCards: KCNH5
Genetically Related Diseases
major depressive disorder
Targeted by Drug
quinidine
RNA expression pattern
PBB GE KCNH5 gnf1h06293 at fs.png

PBB GE KCNH5 gnf1h09304 at fs.png

PBB GE KCNH5 gnf1h08083 at fs.png
More reference expression data
Orthologs
Species Human Mouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_139318
NM_172375
NM_172376

NM_172805

RefSeq (protein)

NP_647479
NP_758963

NP_766393.2
NP_766393

Location (UCSC) Chr 14: 62.7 – 63.1 Mb Chr 12: 74.9 – 75.18 Mb
PubMed search

NM_139318
NM_172375
NM_172376

NM_172805

NP_647479
NP_758963

NP_766393.2
NP_766393

Potassium voltage-gated channel, subfamily H (eag-related), member 5, also known as KCNH5, is a human gene encoding the Kv10.2 protein.

Voltage-gated potassium (Kv) channels represent the most complex class of voltage-gated ion channels from both functional and structural standpoints. Their diverse functions include regulating neurotransmitter release, heart rate, insulin secretion, neuronal excitability, epithelial electrolyte transport, smooth muscle contraction, and cell volume. This gene encodes a member of the potassium channel, voltage-gated, subfamily H. This member is a pore-forming (alpha) subunit of a voltage-gated non-inactivating delayed rectifier potassium channel. This gene is not expressed in differentiating myoblasts. Alternative splicing results in three transcript variants encoding distinct isoforms.


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