CDH17

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

Cadherin-17 is a protein that in humans is encoded by the CDH17 gene.[5][6][7]

AliasesCDH17, CDH16, HPT-1, HPT1, cadherin 17
End94,217,303 bp[1]
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CDH17
Identifiers
AliasesCDH17, CDH16, HPT-1, HPT1, cadherin 17
External IDsOMIM: 603017; MGI: 1095414; HomoloGene: 56859; GeneCards: CDH17; OMA:CDH17 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001144663
NM_004063

NM_019753

RefSeq (protein)

NP_001138135
NP_004054

NP_062727

Location (UCSC)Chr 8: 94.13 – 94.22 MbChr 4: 11.76 – 11.82 Mb
PubMed search[3][4]
Wikidata
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This gene is a member of the cadherin superfamily, genes encoding calcium-dependent, membrane-associated glycoproteins. The encoded protein is cadherin-like, consisting of an extracellular region, containing 7 cadherin domains, and a transmembrane region but lacking the conserved cytoplasmic domain. The protein is a component of the gastrointestinal tract and pancreatic ducts, acting as an intestinal proton-dependent peptide transporter in the first step in oral absorption of many medically important peptide-based drugs. The protein may also play a role in the morphological organization of liver and intestine.[7]

References

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