CLCA1

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

Chloride channel accessory 1 is a protein that in humans is encoded by the CLCA1 gene.[5][6]

AliasesCLCA1, CACC, CACC1, CLCRG1, CaCC-1, GOB5, hhCaCC-1, chloride channel accessory 1
End86,500,259 bp[1]
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CLCA1
Identifiers
AliasesCLCA1, CACC, CACC1, CLCRG1, CaCC-1, GOB5, hhCaCC-1, chloride channel accessory 1
External IDsOMIM: 603906; MGI: 1346342; HomoloGene: 984; GeneCards: CLCA1; OMA:CLCA1 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001285

NM_017474

RefSeq (protein)

NP_001276

NP_059502

Location (UCSC)Chr 1: 86.47 – 86.5 MbChr 3: 144.71 – 144.74 Mb
PubMed search[3][4]
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This gene encodes a member of the calcium sensitive chloride conductance protein family. To date, all members of this gene family map to the same region on chromosome 1p31-p22 and share a high degree of homology in size, sequence, and predicted structure, but differ significantly in their tissue distributions. The encoded protein is expressed as a precursor protein that is processed into two cell-surface-associated subunits, although the site at which the precursor is cleaved has not been precisely determined. The encoded protein may be involved in mediating calcium-activated chloride conductance in the intestine.[6] Protein structure prediction methods suggest the N-terminal region of CLCA1 protein is a zinc metalloprotease.[7]

See also

References

Further reading

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