KCNG1

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

Potassium voltage-gated channel subfamily G member 1 is a protein that in humans is encoded by the KCNG1 gene.[5][6][7]

AliasesKCNG1, K13, KCNG, KV6.1, kH2, potassium voltage-gated channel modifier subfamily G member 1
End51,023,107 bp[1]
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KCNG1
Identifiers
AliasesKCNG1, K13, KCNG, KV6.1, kH2, potassium voltage-gated channel modifier subfamily G member 1
External IDsOMIM: 603788; MGI: 3616086; HomoloGene: 20515; GeneCards: KCNG1; OMA:KCNG1 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_002237
NM_172318

NM_001081134
NM_001379458

RefSeq (protein)

NP_002228

NP_001074603
NP_001366387

Location (UCSC)Chr 20: 51 – 51.02 MbChr 2: 168.1 – 168.12 Mb
PubMed search[3][4]
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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 G. This gene is abundantly expressed in skeletal muscle. Alternative splicing results in at least two transcript variants encoding distinct isoforms.[7]

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