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KCNK1

From Wikipedia, the free encyclopedia
Protein-coding gene in the species Homo sapiens
KCNK1
Available structures
PDBOrtholog search:PDBeRCSB
List of PDB id codes

3UKM

Identifiers
AliasesKCNK1, DPK, HOHO, K2P1, K2p1.1, KCNO1, TWIK-1, TWIK1, potassium two pore domain channel subfamily K member 1
External IDsOMIM:601745;MGI:109322;HomoloGene:1691;GeneCards:KCNK1;OMA:KCNK1 - orthologs
Gene location (Human)
Chromosome 1 (human)
Chr.Chromosome 1 (human)[1]
Chromosome 1 (human)
Genomic location for KCNK1
Genomic location for KCNK1
Band1q42.2Start233,614,106bp[1]
End233,672,514bp[1]
Gene location (Mouse)
Chromosome 8 (mouse)
Chr.Chromosome 8 (mouse)[2]
Chromosome 8 (mouse)
Genomic location for KCNK1
Genomic location for KCNK1
Band8|8 E2Start126,721,909bp[2]
End126,757,424bp[2]
RNA expression pattern
Bgee
HumanMouse (ortholog)
Top expressed in
  • cerebellar vermis

  • pons

  • endothelial cell

  • cerebellar hemisphere

  • orbitofrontal cortex

  • right hemisphere of cerebellum

  • paraflocculus of cerebellum

  • cartilage tissue

  • corpus epididymis

  • cardiac muscle tissue of right atrium
Top expressed in
  • seminal vesicula

  • molar

  • choroid plexus of fourth ventricle

  • lobe of cerebellum

  • lobe of prostate

  • mucosa of urinary bladder

  • transitional epithelium of urinary bladder

  • cerebellar vermis

  • Epithelium of choroid plexus

  • submandibular gland
More reference expression data
BioGPS
n/a
Gene ontology
Molecular function
Cellular component
Biological process
Sources:Amigo /QuickGO
Orthologs
SpeciesHumanMouse
Entrez

3775

16525

Ensembl

ENSG00000135750

ENSMUSG00000033998

UniProt

O00180

O08581

RefSeq (mRNA)

NM_002245

NM_008430

RefSeq (protein)

NP_002236

NP_032456

Location (UCSC)Chr 1: 233.61 – 233.67 MbChr 8: 126.72 – 126.76 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Potassium channel subfamily K member 1 is aprotein that in humans is encoded by theKCNK1gene.[5][6][7]

This gene encodes K2P1.1, a member of the superfamily ofpotassium channelproteins containing two pore-forming P domains. The product of this gene has not been shown to be a functional channel, however, and it may require other non-pore-forming proteins for activity.[7]

See also

[edit]

References

[edit]
  1. ^abcGRCh38: Ensembl release 89: ENSG00000135750Ensembl, May 2017
  2. ^abcGRCm38: Ensembl release 89: ENSMUSG00000033998Ensembl, 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. ^Lesage F, Mattei M, Fink M, Barhanin J, Lazdunski M (Dec 1996). "Assignment of the human weak inward rectifier K+ channel TWIK-1 gene to chromosome 1q42-q43".Genomics.34 (1):153–5.doi:10.1006/geno.1996.0259.PMID 8661042.
  6. ^Goldstein SA, Bayliss DA, Kim D, Lesage F, Plant LD, Rajan S (Dec 2005)."International Union of Pharmacology. LV. Nomenclature and molecular relationships of two-P potassium channels".Pharmacol Rev.57 (4):527–40.doi:10.1124/pr.57.4.12.PMID 16382106.S2CID 7356601.
  7. ^ab"Entrez Gene: KCNK1 potassium channel, subfamily K, member 1".

Further reading

[edit]

External links

[edit]

This article incorporates text from theUnited States National Library of Medicine, which is in thepublic domain.

Ligand-gated
Voltage-gated
Constitutively active
Proton-gated
Voltage-gated
Calcium-activated
Inward-rectifier
Tandem pore domain
Voltage-gated
Miscellaneous
Cl:Chloride channel
H+:Proton channel
M+:CNG cation channel
M+:TRP cation channel
H2O (+solutes):Porin
Cytoplasm:Gap junction
By gating mechanism
Ion channel class
see alsodisorders
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