Gene: Kcnv2 (potassium voltage-gated channel modifier subfamily V member 2) Rattus norvegicus
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Symbol: Kcnv2
Name: potassium voltage-gated channel modifier subfamily V member 2
Description: INVOLVED IN protein homooligomerization (inferred); regulation of ion transmembrane transport (inferred); ASSOCIATED WITH cone dystrophy (ortholog); Cone Dystrophy 3 (ortholog); dystrophies primarily involving the retinal pigment epithelium (ortholog); FOUND IN voltage-gated potassium channel complex (inferred); INTERACTS WITH bisphenol A; 1,1,1-trichloroethane (ortholog); 2,3,7,8-tetrachlorodibenzodioxine (ortholog)
Type: protein-coding
RefSeq Status: PROVISIONAL
Also known as: LOC294065; potassium channel, subfamily V, member 2; potassium channel, voltage-gated modifier subfamily V, member 2; potassium voltage-gated channel subfamily V member 2
Orthologs:
Latest Assembly: Rnor_6.0 - RGSC Genome Assembly v6.0
Position:
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Rnor_6.01245,396,880 - 245,475,011 (+)NCBIRnor6.0rn6Rnor6.0
Rnor_5.01252,646,135 - 252,663,285 (+)NCBIRnor5.0rn5Rnor5.0
RGSC_v3.41230,834,883 - 230,849,285 (+)NCBIRGSC3.4rn4RGSC3.4
RGSC_v3.11230,999,015 - 231,009,903 (+)NCBI
Celera1222,175,534 - 222,189,894 (+)NCBI
Cytogenetic Map1q52NCBImapview
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations
Gene-Chemical Interaction Annotations
Gene Ontology Annotations
References - curated
References - uncurated
RGD Disease Portals

Genomics

Comparative Map Data
Position Markers
QTLs in Region (Rnor_6.0)
miRNA Target Status

Sequence

Nucleotide Sequences
Protein Sequences
Transcriptome

Strain Variation

Strain Sequence Variants

Additional Information

External Database Links
Nomenclature History
 
More on Kcnv2
NCBI Gene
Ensembl Gene
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RGD Object Information
RGD ID: 1309271
Created: 2005-01-12
Species: Rattus norvegicus
Last Modified: 2017-05-30
Status: ACTIVE