CLCA2

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

Chloride channel accessory 2 is a protein that in humans is encoded by the CLCA2 gene.[5]

AliasesCLCA2, CACC, CACC3, CLCRG2, CaCC-3, chloride channel accessory 2
End86,456,553 bp[1]
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CLCA2
Identifiers
AliasesCLCA2, CACC, CACC3, CLCRG2, CaCC-3, chloride channel accessory 2
External IDsOMIM: 604003; MGI: 2139758; HomoloGene: 4765; GeneCards: CLCA2; OMA:CLCA2 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_006536

NM_178697

RefSeq (protein)

NP_006527

NP_848812

Location (UCSC)Chr 1: 86.42 – 86.46 MbChr 3: 144.78 – 144.81 Mb
PubMed search[3][4]
Wikidata
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The protein encoded by this gene belongs to the calcium sensitive chloride conductance protein family. To date, all members of this gene family map to the same site on chromosome 1p31-p22 and share high degrees of homology in size, sequence and predicted structure, but differ significantly in their tissue distributions. Since this protein is expressed predominantly in trachea and lung, it is suggested to play a role in the complex pathogenesis of cystic fibrosis. It may also serve as adhesion molecule for lung metastatic cancer cells, mediating vascular arrest and colonization, and furthermore, it has been implicated to act as a tumor suppressor gene for breast cancer.[5] Protein structure prediction methods suggest the N-terminal region of CLCA2 protein is a zinc metalloprotease.[6]

See also

References

Further reading

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