Entity Details

Primary name IF_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionP27352
EntryNameIF_HUMAN
FullNameCobalamin binding intrinsic factor
TaxID9606
Evidenceevidence at protein level
Length417
SequenceStatuscomplete
DateCreated1992-08-01
DateModified2021-06-02

Ontological Relatives

GenesCBLIF

GO terms

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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

Subcellular Location

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Subcellular Location
Secreted

Domains

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DomainNameCategoryType
IPR002157 Cobalamin (vitamin B12)-binding proteinFamilyFamily
IPR027954 Domain of unknown function DUF4430DomainDomain

Diseases

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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.

Drugs

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DrugNameSourceType
DB00115 CyanocobalaminDrugbanksmall molecule