Entity Details

Primary name CBLIF
Entity type gene
Source Source Link

Details

PrimaryID2694
RefseqGeneNG_008120
SymbolCBLIF
Namecobalamin binding intrinsic factor
Chromosome11
Location11q12.1
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate1991-06-27
ModificationDate2021-06-11

Ontological Relatives

UniProt IDsIF_HUMAN

GO terms

Show/Hide Table
GOName
GO:0005576 extracellular region
GO:0005615 extracellular space
GO:0005768 endosome
GO:0005902 microvillus
GO:0006824 cobalt ion transport
GO:0009235 cobalamin metabolic process
GO:0015889 cobalamin transport
GO:0016324 apical plasma membrane
GO:0031419 cobalamin binding
GO:0043202 lysosomal lumen

Diseases

Show/Hide Table
Disease IDSourceNameDescription
261000 OMIMHereditary intrinsic factor deficiency (IFD)Autosomal recessive disorder characterized by megaloblastic anemia. The disease is caused by variants affecting the gene represented in this entry.

Interactions

13 interactions

InteractorPartnerSourcesPublicationsLink
CBLIFCUBNBioGRID, DIP, HPRD20237569 9572993 details
CBLIFSLC7A14BioGRID, IntAct32296183 details
CBLIFSLC7A1BioGRID, IntAct32296183 details
CBLIFSLC13A4BioGRID, IntAct32296183 details
CBLIFTMEM237BioGRID, IntAct32296183 details
CBLIFSLC22A23BioGRID, IntAct32296183 details
CBLIFFFAR2BioGRID, IntAct32296183 details
CBLIFCBLIFDIP17954916 details
CBLIFCBLBioGRID11788601 details
CBLIFATP4ABioGRID17255364 details
CBLIFGALNT5BioGRID, IntAct28514442 details
CBLIFFBXO2BioGRID, IntAct28514442 details
CBLIFHSPA8BioGRID, IntAct30021884 details