KCNV1

Protein-coding gene in the species Homo sapiens
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
Gene location (Human)
Chromosome 8 (human)
Chr.Chromosome 8 (human)[1]
Chromosome 8 (human)
Genomic location for KCNV1
Genomic location for KCNV1
Band8q23.2Start109,963,636 bp[1]
End109,975,771 bp[1]
Gene location (Mouse)
Chromosome 15 (mouse)
Chr.Chromosome 15 (mouse)[2]
Chromosome 15 (mouse)
Genomic location for KCNV1
Genomic location for KCNV1
Band15|15 B3.3Start44,969,680 bp[2]
End44,978,316 bp[2]
RNA expression pattern
Bgee
HumanMouse (ortholog)
Top expressed in
  • prefrontal cortex

  • endothelial cell

  • dorsolateral prefrontal cortex

  • Brodmann area 9

  • superior frontal gyrus

  • Brodmann area 23

  • Brodmann area 46

  • cingulate gyrus

  • middle temporal gyrus

  • orbitofrontal cortex
Top expressed in
  • prefrontal cortex

  • primary motor cortex

  • superior frontal gyrus

  • piriform cortex

  • temporal lobe

  • hippocampus proper

  • cingulate gyrus

  • amygdala

  • nucleus accumbens

  • Region I of hippocampus proper
More reference expression data
BioGPS
n/a
Gene ontology
Molecular function
  • ion channel inhibitor activity
  • potassium channel regulator activity
  • ion channel activity
  • voltage-gated ion channel activity
  • potassium channel activity
  • voltage-gated potassium channel activity
Cellular component
  • plasma membrane
  • membrane
  • voltage-gated potassium channel complex
  • integral component of membrane
  • integral component of plasma membrane
Biological process
  • ion transport
  • transmembrane transport
  • potassium ion transport
  • protein homooligomerization
  • regulation of ion transmembrane transport
  • potassium ion transmembrane transport
Sources:Amigo / QuickGO
Orthologs
SpeciesHumanMouse
Entrez

27012

67498

Ensembl

ENSG00000164794

ENSMUSG00000022342

UniProt

Q6PIU1

Q8BZN2

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
View/Edit HumanView/Edit Mouse

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]

Common variations in the KCNV1 gene have been associated with schizophrenia.[7]

References

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000164794 – Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000022342 – Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ a b Hugnot JP, Salinas M, Lesage F, Guillemare E, de Weille J, Heurteaux C, Mattei MG, Lazdunski M (Aug 1996). "Kv8.1, a new neuronal potassium channel subunit with specific inhibitory properties towards Shab and Shaw channels". EMBO J. 15 (13): 3322–31. doi:10.1002/j.1460-2075.1996.tb00697.x. PMC 451895. PMID 8670833.
  6. ^ a b Gutman GA, Chandy KG, Grissmer S, Lazdunski M, McKinnon D, Pardo LA, Robertson GA, Rudy B, Sanguinetti MC, Stuhmer W, Wang X (Dec 2005). "International Union of Pharmacology. LIII. Nomenclature and molecular relationships of voltage-gated potassium channels". Pharmacol Rev. 57 (4): 473–508. doi:10.1124/pr.57.4.10. PMID 16382104. S2CID 219195192.
  7. ^ Schizophrenia Working Group of the Psychiatric Genomics Consortium (2014-07-24). "Biological insights from 108 schizophrenia-associated genetic loci". Nature. 511 (7510): 421–427. Bibcode:2014Natur.511..421S. doi:10.1038/nature13595. ISSN 1476-4687. PMC 4112379. PMID 25056061.

Further reading

  • Strausberg RL, Feingold EA, Grouse LH, et al. (2002). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. Bibcode:2002PNAS...9916899M. doi:10.1073/pnas.242603899. PMC 139241. PMID 12477932.
  • Sano A, Mikami M, Nakamura M, et al. (2002). "Positional candidate approach for the gene responsible for benign adult familial myoclonic epilepsy". Epilepsia. 43 (Suppl 9): 26–31. doi:10.1046/j.1528-1157.43.s.9.7.x. PMID 12383276. S2CID 39236204.
  • Ebihara M, Ohba H, Kikuchi M, Yoshikawa T (2004). "Structural characterization and promoter analysis of human potassium channel Kv8.1 (KCNV1) gene". Gene. 325: 89–96. doi:10.1016/j.gene.2003.09.044. PMID 14697513.
  • Salinas M, de Weille J, Guillemare E, et al. (1997). "Modes of regulation of shab K+ channel activity by the Kv8.1 subunit". J. Biol. Chem. 272 (13): 8774–80. doi:10.1074/jbc.272.13.8774. PMID 9079713.

External links

  • v
  • t
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Ligand-gated
Voltage-gated
Constitutively active
Proton-gated
Voltage-gated
Calcium-activated
Inward-rectifier
Tandem pore domain
Voltage-gated
Miscellaneous
Cl: Chloride channel
H+: Proton channel
M+: CNG cation channel
M+: TRP cation channel
H2O (+ solutes): Porin
Cytoplasm: Gap junction
By gating mechanism
Ion channel class
see also disorders


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