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CBLIF

Gene

cobalamin binding intrinsic factor

HGNCHGNC:4268EnsemblENSG00000134812NCBI Gene2694
Locus: gene with protein productLocation: 11q12.1

Also known as

Symbols and names change; identity (the HGNC ID) does not. Previous and alternative forms are kept distinct.

Also known asGIF · TCN3 · IF · IFMH · INF
View full nomenclature history (7)
Previous symbolsGIF
Alias symbolsTCN3, IF, IFMH, INF
Previous namesgastric intrinsic factor (vitamin B synthesis), gastric intrinsic factor

Associated diseases

via associated_with

Diseases linked to this gene through the canonical GENE→DISEASE (associated_with) relation, drawn from Open Targets' top-ranked associations by overall score — not the full association set. Disease-level detail lives on each disease's own page.

Vitamin B Deficiency
Gastric carcinoma

Drawn from Open Targets’ top 10 associations by overall score for this gene — the subset resolved to a canonical disease. Lower-ranked associations, and diseases not yet canonicalised, are not shown.

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-01-20.
Open TargetsGene–disease associations from the Open Targets Platform.