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 3 (ortholog); Retinal Cone Dystrophy 3B (ortholog); Retinal Dystrophies (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 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_5.01252,646,135 - 252,663,285 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
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 (+)NCBICelera
Cytogenetic Map1q52NCBI
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
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: rn5 rn6
NCBI Genome Data Viewer

RGD Object Information
RGD ID: 1309271
Created: 2005-01-12
Species: Rattus norvegicus
Last Modified: 2018-02-06
Status: ACTIVE