KCNV2

KCNV2
Identifiers
Aliases	KCNV2, KV11.1, Kv8.2, RCD3B, potassium voltage-gated channel modifier subfamily V member 2
External IDs	OMIM: 607604; MGI: 2670981; HomoloGene: 26423; GeneCards: KCNV2; OMA:KCNV2 - orthologs
Gene location (Human)
Chr.	Chromosome 9 (human)
End	2,730,037 bp
Gene location (Mouse)
Chr.	Chromosome 19 (mouse)
End	27,314,579 bp
RNA expression pattern
	Top expressed in
	sperm; ; testicle; ; gonad; ; retinal pigment epithelium; ; right testis; ; left testis; ; sural nerve; ; pancreatic ductal cell; ; right hemisphere of cerebellum; ; ganglionic eminence;
	Top expressed in
	neural layer of retina; ; outer nuclear layer; ; embryo; ; blastocyst; ; gastrula; ; lumbar subsegment of spinal cord; ; inner nuclear layer; ; zygote; ; lumbar spinal ganglion; ; sternocleidomastoid muscle;
	More reference expression data
	n/a
Gene ontology
Molecular function	ion channel activity; potassium channel activity; voltage-gated ion channel activity; voltage-gated potassium channel activity;
Cellular component	integral component of membrane; voltage-gated potassium channel complex; plasma membrane; membrane;
Biological process	potassium ion transport; regulation of ion transmembrane transport; protein homooligomerization; ion transport; transmembrane transport; potassium ion transmembrane transport;
	Sources:Amigo / QuickGO
Orthologs
	169522
	240595
	ENSG00000168263
	ENSMUSG00000047298
	Q8TDN2
	Q8CFS6
	NM_133497
	NM_183179
	NP_598004
	NP_899002
	Wikidata
View/Edit Human	View/Edit Mouse

Potassium voltage-gated channel subfamily V member 2 is a protein that in humans is encoded by the KCNV2 gene. The protein encoded by this gene is a voltage-gated potassium channel subunit.