CDH3 (gene)

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

CDH3 (gene)

Cadherin-3, also known as P-Cadherin, is a protein that in humans is encoded by the CDH3 gene.[5][6]

Quick Facts Available structures, PDB ...
CDH3
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesCDH3, CDHP, HJMD, PCAD, cadherin 3
External IDsOMIM: 114021; MGI: 88356; HomoloGene: 20425; GeneCards: CDH3; OMA:CDH3 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001793
NM_001317195
NM_001317196

NM_001037809
NM_007665

RefSeq (protein)

NP_001304124
NP_001304125
NP_001784

NP_001032898
NP_031691

Location (UCSC)Chr 16: 68.64 – 68.73 MbChr 8: 107.24 – 107.28 Mb
PubMed search[3][4]
Wikidata
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Function

This gene is a classical cadherin from the cadherin superfamily. The encoded protein is a calcium-dependent cell-cell adhesion glycoprotein composed of five extracellular cadherin repeats, a transmembrane region and a highly conserved cytoplasmic tail. This gene is located in a six-cadherin cluster in a region on the long arm of chromosome 16 that is involved in loss of heterozygosity events in breast and prostate cancer. In addition, aberrant expression of this protein is observed in cervical adenocarcinomas.

Clinical significance

Mutations in this gene have been associated with congenital hypotrichosis with juvenile macular dystrophy.[6]

Interactions

CDH3 (gene) has been shown to interact with:

History

Cadherin-3 was first described in 1986 by Masatoshi Takeichi's laboratory as a new cadherin molecule most abundant in the developing mouse placenta – hence "P-cadherin".[10][11]

See also

References

Further reading

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