KCNV1

KCNV1
Identifiers
Aliases	KCNV1, HNKA, KCNB3, KV2.3, KV8.1, potassium voltage-gated channel modifier subfamily V member 1
External IDs	OMIM: 608164; MGI: 1914748; HomoloGene: 22811; GeneCards: KCNV1; OMA:KCNV1 - orthologs
Gene location (Human)
Chr.	Chromosome 8 (human)
End	109,975,771 bp
Gene location (Mouse)
Chr.	Chromosome 15 (mouse)
End	44,978,316 bp
RNA expression pattern
	Top expressed in
	buccal mucosa cell; ; prefrontal cortex; ; endothelial cell; ; dorsolateral prefrontal cortex; ; Brodmann area 9; ; superior frontal gyrus; ; right frontal lobe; ; Brodmann area 23; ; Brodmann area 46; ; cingulate gyrus;
	Top expressed in
	lumbar spinal ganglion; ; prefrontal cortex; ; primary motor cortex; ; superior frontal gyrus; ; primary visual cortex; ; piriform cortex; ; dentate gyrus of hippocampal formation granule cell; ; temporal lobe; ; hippocampus proper; ; cingulate gyrus;
	More reference expression data
	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
	27012
	67498
	ENSG00000164794
	ENSMUSG00000022342
	Q6PIU1
	Q8BZN2
	NM_014379
	NM_026200
	NP_055194
	NP_080476
	Wikidata
View/Edit Human	View/Edit Mouse

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

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