KCNV1

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

KCNV1

Potassium voltage-gated channel subfamily V member 1 is a protein that in humans is encoded by the KCNV1 gene.[5][6] The protein encoded by this gene is a voltage-gated potassium channel subunit.[5][6]

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KCNV1
Identifiers
AliasesKCNV1, HNKA, KCNB3, KV2.3, KV8.1, potassium voltage-gated channel modifier subfamily V member 1
External IDsOMIM: 608164; MGI: 1914748; HomoloGene: 22811; GeneCards: KCNV1; OMA:KCNV1 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_014379

NM_026200

RefSeq (protein)

NP_055194

NP_080476

Location (UCSC)Chr 8: 109.96 – 109.98 MbChr 15: 44.97 – 44.98 Mb
PubMed search[3][4]
Wikidata
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Common variations in the KCNV1 gene have been associated with schizophrenia.[7]

References

Further reading

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