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Gene id 169522
Gene Summary    Protein Summary    Gene ontology    Diseases    PubMed    

Gene Summary

Gene Symbol KCNV2   Gene   UCSC   Ensembl
Aliases KV11.1, Kv8.2, RCD3B
Gene name potassium voltage-gated channel modifier subfamily V member 2
Alternate names potassium voltage-gated channel subfamily V member 2, potassium channel, subfamily V, member 2, potassium channel, voltage gated modifier subfamily V, member 2, voltage-gated potassium channel subunit Kv8.2,
Gene location 9p24.2 (2717509: 2730036)     Exons: 2     NC_000009.12
Gene summary(Entrez) 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, neuro

Protein Summary

Protein general information Q8TDN2  

Name: Potassium voltage gated channel subfamily V member 2 (Voltage gated potassium channel subunit Kv8.2)

Length: 545  Mass: 62459

Tissue specificity: Detected in lung, liver, kidney, pancreas, spleen, thymus, prostate, testis, ovary and colon. {ECO

Sequence MLKQSERRRSWSYRPWNTTENEGSQHRRSICSLGARSGSQASIHGWTEGNYNYYIEEDEDGEEEDQWKDDLAEED
QQAGEVTTAKPEGPSDPPALLSTLNVNVGGHSYQLDYCELAGFPKTRLGRLATSTSRSRQLSLCDDYEEQTDEYF
FDRDPAVFQLVYNFYLSGVLLVLDGLCPRRFLEELGYWGVRLKYTPRCCRICFEERRDELSERLKIQHELRAQAQ
VEEAEELFRDMRFYGPQRRRLWNLMEKPFSSVAAKAIGVASSTFVLVSVVALALNTVEEMQQHSGQGEGGPDLRP
ILEHVEMLCMGFFTLEYLLRLASTPDLRRFARSALNLVDLVAILPLYLQLLLECFTGEGHQRGQTVGSVGKVGQV
LRVMRLMRIFRILKLARHSTGLRAFGFTLRQCYQQVGCLLLFIAMGIFTFSAAVYSVEHDVPSTNFTTIPHSWWW
AAVSISTVGYGDMYPETHLGRFFAFLCIAFGIILNGMPISILYNKFSDYYSKLKAYEYTTIRRERGEVNFMQRAR
KKIAECLLGSNPQLTPRQEN
Structural information
Interpro:  IPR005821  IPR003968  IPR003971  IPR011333  IPR003131  
IPR028325  IPR027359  
STRING:   ENSP00000371514
Other Databases GeneCards:  KCNV2  Malacards:  KCNV2

Gene ontology

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GO accessionTerm nameEvidence codeGo category
GO:0005249 voltage-gated potassium c
hannel activity
IBA molecular function
GO:0005249 voltage-gated potassium c
hannel activity
IBA molecular function
GO:0008076 voltage-gated potassium c
hannel complex
IBA cellular component
GO:0016021 integral component of mem
brane
IBA cellular component
GO:0071805 potassium ion transmembra
ne transport
IBA biological process
GO:0005216 ion channel activity
IEA molecular function
GO:0005249 voltage-gated potassium c
hannel activity
IEA molecular function
GO:0006811 ion transport
IEA biological process
GO:0006813 potassium ion transport
IEA biological process
GO:0008076 voltage-gated potassium c
hannel complex
IEA cellular component
GO:0016020 membrane
IEA cellular component
GO:0051260 protein homooligomerizati
on
IEA biological process
GO:0055085 transmembrane transport
IEA biological process
GO:0005244 voltage-gated ion channel
activity
IEA molecular function
GO:0005267 potassium channel activit
y
IEA molecular function
GO:0071805 potassium ion transmembra
ne transport
IEA biological process
GO:0006811 ion transport
IEA biological process
GO:0016020 membrane
IEA cellular component
GO:0034765 regulation of ion transme
mbrane transport
IEA biological process
GO:0005886 plasma membrane
IEA cellular component
GO:0006813 potassium ion transport
IEA biological process
GO:0016021 integral component of mem
brane
IEA cellular component
GO:0005886 plasma membrane
TAS cellular component
GO:0005515 protein binding
IPI molecular function
GO:0005886 plasma membrane
IEA cellular component
Associated diseases References
Cone-rod dystrophy and cone dystrophy KEGG:H00481
Cone-rod dystrophy and cone dystrophy KEGG:H00481
Aberrant CpGs in Low Motility Sperm MIK: 21674046

PubMed references

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PMID Condition Mutation Ethnicity Population details Infertility_type Associated_genes Abstract
21674046 Aberrant C
pGs in Low
Motility
Sperm

18
Male infertility GSE26881
Show abstract