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Cubilin

Mammalian protein found in humans From Wikipedia, the free encyclopedia

Cubilin is a protein that in humans is encoded by the CUBN gene.[5][6][7] It is present upon the luminal surface of enterocytes of the ileum where it facilitates absorption of vitamin B12 by acting as a receptor for IF-cobalamin (intrinsic factor - vitamin B12) complexes, enabling endocytosis of complexes by means of amnionless (AMN).[8][9]

AliasesCUBN, IFCR, MGA1, gp280, cubilin, IGS, IGS1
External IDsOMIM: 602997; MGI: 1931256; GeneCards: CUBN
PDBOrtholog search: PDBe RCSB
Quick facts CUBN, Identifiers ...
CUBN
Identifiers
AliasesCUBN, IFCR, MGA1, gp280, cubilin, IGS, IGS1
External IDsOMIM: 602997; MGI: 1931256; GeneCards: CUBN
Available structures
PDBOrtholog search: PDBe RCSB
Orthologs
DatabasesNCBI: entry; OMA: entry
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001081

NM_001081084

RefSeq (protein)

NP_001072

NP_001074553

Location (UCSC)Chr 10: 16.82 – 17.13 MbChr 2: 13.28 – 13.5 Mb
PubMed search[3][4]
Wikidata
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Biochemistry

Cubilinis essentially only present in the small intestine and kidneys.[10]

A complex of amnionless and cubilin forms the cubam receptor.[11]

Clinical significance

Mutations in CUBN may play a role in autosomal recessive megaloblastic anemia.[7]

Cubilin is a potential diagnostic and prognostic cancer biomarker for kidney cancer.[12] Based on patient survival data, high levels of cubilin in tumor cells is a favourable prognostic biomarker in renal cell carcinoma.[13][14]

References

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