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Link to original content: http://en.wikipedia.org/wiki/Kv3.4
KCNC4 - Wikipedia Jump to content

KCNC4

From Wikipedia, the free encyclopedia
(Redirected from Kv3.4)
KCNC4
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesKCNC4, C1orf30, HKSHIIIC, KSHIIIC, KV3.4, potassium voltage-gated channel subfamily C member 4
External IDsOMIM: 176265; MGI: 96670; HomoloGene: 68427; GeneCards: KCNC4; OMA:KCNC4 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001039574
NM_004978
NM_153763
NM_001377330
NM_001377331

NM_145922
NM_001356447

RefSeq (protein)

NP_001034663
NP_004969
NP_001364259
NP_001364260

NP_666034
NP_001343376

Location (UCSC)Chr 1: 110.21 – 110.28 MbChr 3: 107.35 – 107.37 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Potassium voltage-gated channel, Shaw-related subfamily, member 4 (KCNC4), also known as Kv3.4, is a human gene.[5]

The Shaker gene family of Drosophila encodes components of voltage-gated potassium channels and comprises four subfamilies. Based on sequence similarity, this gene is similar to the Shaw subfamily. The protein encoded by this gene belongs to the delayed rectifier class of channel proteins and is an integral membrane protein that mediates the voltage-dependent potassium ion permeability of excitable membranes. It generates atypical voltage-dependent transient current that may be important for neuronal excitability. Several transcript variants encoding different isoforms have been found for this gene.[5]

See also

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References

[edit]
  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000116396Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000027895Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ a b "Entrez Gene: KCNC4 potassium voltage-gated channel, Shaw-related subfamily, member 4".

Further reading

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This article incorporates text from the United States National Library of Medicine, which is in the public domain.