Gene: KCNS3 (potassium voltage-gated channel, delayed-rectifier, subfamily S, member 3)  Homo sapiens

Symbol: KCNS3
Name: potassium voltage-gated channel, delayed-rectifier, subfamily S, member 3
Description: Voltage-gated potassium channels form the largest and most diversified class of ion channels and are present in both excitable and nonexcitable cells. Their main functions are associated with the regulation of the resting membrane potential and the control of the shape and frequency of action potentials. The alpha subunits are of 2 types: those that are functional by themselves and those that are electrically silent but capable of modulating the activity of specific functional alpha subunits. The protein encoded by this gene is not functional by itself but can form heteromultimers with member 1 and with member 2 (and possibly other members) of the Shab-related subfamily of potassium voltage-gated channel proteins. This gene belongs to the S subfamily of the potassium channel family. [provided by RefSeq, Jul 2008]
Type: protein-coding
RefSeq Status: REVIEWED
Also known as: delayed-rectifier K(+) channel alpha subunit 3; KV9.3; MGC9481; OTTHUMP00000149986; OTTHUMP00000200487; potassium voltage-gated channel delayed-rectifier protein S3; potassium voltage-gated channel subfamily S member 3; Shab-related delayed-rectifier K+ channel alpha subunit 3; voltage-gated potassium channel protein Kv9.3; voltage-gated potassium channel subunit Kv9.3
Orthologs: Mus musculus : Kcns3 (potassium voltage-gated channel, delayed-rectifier, subfamily S, member 3)  MGI
Rattus norvegicus : Kcns3 (potassium voltage-gated channel, delayed-rectifier, subfamily S, member 3)
Latest Assembly: Human Genome Assembly GRCh37
Position:
MapChrPositionStrandSource
Human Alternate Assembly CHM1_1218,028,149 - 18,082,497+NCBI
Human Genome Assembly HuRef217,834,922 - 17,889,158+NCBI
Human Genome Assembly GRCh37218,059,945 - 18,114,225+NCBI
Human Celera Assembly217,940,636 - 17,994,899+NCBI
Human Genome Assembly Build 36217,923,426 - 17,977,706+NCBI
Human Cytogenetic Map2p24 NCBI
Human Genome Assembly217,981,572 - 18,035,852 NCBI
Model

Launch Genome Browser (GBrowse) : build 36 (hg18) build 37 (hg19)


References - curated
References - uncurated
RGD Disease Portals

Genomics

Comparative Map Data
Position Markers
QTLs in Region (Human Genome Assembly GRCh37)

Sequence

Nucleotide Sequences
Protein Sequences
Promoters

Additional Information

External Database Links
Nomenclature History
 
More on KCNS3
Entrez Gene
Ensembl Gene
Genome Browser: (hg18) (hg19)
HGNC Report
NCBI Map Viewer
Vista
Vista + UCSC

RGD Object Information
RGD ID: 731286
Created: 2004-01-12
Species: Homo sapiens
Last Modified: 2013-03-05
Status: ACTIVE