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Protein Coding Gene : Kcns2 K+ voltage-gated channel, subfamily S, 2

Primary Identifier  MGI:1197011 Organism  mouse, laboratory
Chromosome  15 NCBI Gene Number  16539
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 8.0.0)

Enables potassium channel regulator activity. Involved in potassium ion transport and regulation of potassium ion transmembrane transport. Located in perinuclear region of cytoplasm and plasma membrane. Part of voltage-gated potassium channel complex. Is expressed in diencephalon lateral wall mantle layer; heart; and olfactory epithelium. Orthologous to human KCNS2 (potassium voltage-gated channel modifier subfamily S member 2).
PHENOTYPE: Homozygous mutation of this gene results in no obvious phenotype. [provided by MGI curators]
  • synonyms:
  • E130006J24Rik,
  • RIKEN cDNA E130006J24 gene,
  • K+ voltage-gated channel, subfamily S, 2,
  • Kv9.2,
  • Kcns2,
  • MGI:2443152

Features --> Cross References

Genome

Sequence Feature Displayer

JG Browse Displayer

0 Canonical

0 CDSs

0 Exons

0 Genomic Clusters

2 Involved In Mutations

0 Strain

0 Transcripts

0 Transgenic Expressors

0 UTRs

Canonical gene --> CDSs in specific strains.

Canonical gene --> Exons in specific strains

Canonical gene --> Strain-specific IDs, biotypes, and locations

Canonical gene --> Transcripts in specific strains.

Features --> Overlapping features

Proteins

Gene --> Proteins

Function

Mouse features --> Functions (GO terms)

Homology

Genes --> Homologs

Interactions

3 Pathways

0 Targeted By

Gene --> Protein-Protein Interactions

Expression

Gene --> Expression annotations

Phenotype

Genes/Features --> Phenotypes (MP terms)

Disease

Mouse features --> Human diseases

Literature

Mouse features --> Publications

 

Other

0 Driver For