GO_REF:0000002
Gene Ontology annotation through association of InterPro records with GO terms
GO_REF:0000033
Annotation inferences using phylogenetic trees
GO_REF:0000044
Gene Ontology annotation based on UniProtKB/Swiss-Prot Subcellular Location vocabulary mapping, accompanied by conservative changes to GO terms applied by UniProt
PMID:14695536
A genetic polymorphism in the coding region of the gastric intrinsic factor gene (GIF) is associated with congenital intrinsic factor deficiency.
PMID:15738392
Hereditary juvenile cobalamin deficiency caused by mutations in the intrinsic factor gene.
PMID:17954916
Crystal structure of human intrinsic factor: cobalamin complex at 2.6-A resolution.
PMID:20237569
Structural basis for receptor recognition of vitamin-B(12)-intrinsic factor complexes.
PMID:32296183
A reference map of the human binary protein interactome.
PMID:8886952
Human gastric intrinsic factor expression is not restricted to parietal cells.
file:human/CBLIF/CBLIF-uniprot.txt
UniProtKB entry P27352 (IF_HUMAN), Cobalamin binding intrinsic factor
Reactome:R-HSA-3000103
CUBN:AMN binds CBLIF:RCbl
Reactome:R-HSA-3000120
CBLIF binds RCbl
Reactome:R-HSA-3000137
CUBN:AMN-mediated CBLIF:RCbl uptake and delivery to lysosome
Reactome:R-HSA-3000243
Unknown lysosomal protease degrades CBLIF:RCbl to release Cbl
Reactome:R-HSA-3296462
Defective CUBN does not transport GIF:Cbl
Reactome:R-HSA-3296477
Defective AMN does not transport GIF:Cbl
Reactome:R-HSA-3315455
Defective CBLIF does not bind Cbl
Reactome:R-HSA-9758881
Uptake of dietary cobalamins into enterocytes