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KCNN1

From Wikipedia, the free encyclopedia
Protein-coding gene in the species Homo sapiens
KCNN1
Identifiers
AliasesKCNN1, KCa2.1, SK1, SKCA1, hSK1, potassium calcium-activated channel subfamily N member 1
External IDsOMIM:602982;MGI:1933993;HomoloGene:37595;GeneCards:KCNN1;OMA:KCNN1 - orthologs
Gene location (Human)
Chromosome 19 (human)
Chr.Chromosome 19 (human)[1]
Chromosome 19 (human)
Genomic location for KCNN1
Genomic location for KCNN1
Band19p13.11Start17,951,293bp[1]
End18,000,080bp[1]
RNA expression pattern
Bgee
HumanMouse (ortholog)
Top expressed in
  • right frontal lobe

  • cingulate gyrus

  • anterior cingulate cortex

  • prefrontal cortex

  • Amygdala

  • Region I of hippocampus proper

  • dorsolateral prefrontal cortex

  • Brodmann area 9

  • ganglionic eminence

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

3780

84036

Ensembl

ENSG00000105642

ENSMUSG00000002908

UniProt

Q92952

Q9EQR3

RefSeq (mRNA)

NM_002248

NM_032397

RefSeq (protein)

NP_002239

NP_115773
NP_001350336
NP_001350337

Location (UCSC)Chr 19: 17.95 – 18 Mbn/a
PubMed search[2][3]
Wikidata
View/Edit HumanView/Edit Mouse

Potassium intermediate/small conductance calcium-activated channel, subfamily N, member 1, also known asKCNN1 is a humangene encoding theKCa2.1protein.[4]

Action potentials in vertebrate neurons are followed by an afterhyperpolarization (AHP) that may persist for several seconds and may have profound consequences for the firing pattern of the neuron. Each component of the AHP is kinetically distinct and is mediated by different calcium-activated potassium channels. The protein encoded by this gene is activated before membrane hyperpolarization and is thought to regulate neuronal excitability by contributing to the slow component of synaptic AHP. The KCa2.1 protein is an integral membrane protein that forms a voltage-independent calcium-activated channel with three other calmodulin-binding subunits. The KCNN1 gene is a member of the KCNN family of potassium channel genes.[4]

See also

[edit]

References

[edit]
  1. ^abcGRCh38: Ensembl release 89: ENSG00000105642Ensembl, May 2017
  2. ^"Human PubMed Reference:".National Center for Biotechnology Information, U.S. National Library of Medicine.
  3. ^"Mouse PubMed Reference:".National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ab"Entrez Gene: KCNN1 potassium intermediate/small conductance calcium-activated channel, subfamily N, member 1".

Further reading

[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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