CALHM1

Protein-coding gene in humans From Wikipedia, the free encyclopedia

Calcium homeostasis modulator 1 (CALHM1) is a pore-forming subunit of a voltage-gated ion channel and a voltage-gated ATP channel that in humans is encoded by the CALHM1 gene.[5][6]

AliasesCALHM1, FAM26C, calcium homeostasis modulator 1
End103,458,900 bp[1]
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CALHM1
Identifiers
AliasesCALHM1, FAM26C, calcium homeostasis modulator 1
External IDsOMIM: 612234; MGI: 3643383; HomoloGene: 55508; GeneCards: CALHM1; OMA:CALHM1 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001001412

NM_001081271

RefSeq (protein)

NP_001001412

NP_001074740

Location (UCSC)Chr 10: 103.45 – 103.46 MbChr 19: 47.13 – 47.13 Mb
PubMed search[3][4]
Wikidata
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Function

Central nervous system

CALHM1 was identified by a tissue-specific gene expression profiling approach[7] that screened for genes located on susceptibility loci for late-onset Alzheimer's disease (AD) and that are preferentially expressed in the hippocampus,[5] a brain region affected early in AD. CALHM1 is a plasma membrane calcium-permeable ion channel regulated by voltage and extracellular calcium levels.[8] The exact function of CALHM1 in the brain is not completely understood, but studies have shown that CALHM1 controls neuronal intracellular calcium homeostasis and signaling, as well as calcium-dependent neuronal excitability and memory in mouse models.[8][9][10] Recent data have also shown that CALHM1 might facilitate the proteolytic degradation of the cerebral amyloid beta peptide, a culprit in AD pathogenesis.[11]

Peripheral taste system

CALHM1 is expressed in taste bud cells where it controls purinergic receptor-mediated taste transduction in the gustatory system.[12][13]

See also

References

Further reading

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