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TGFBI

Gene

transforming growth factor beta induced

HGNCHGNC:11771EnsemblENSG00000120708NCBI Gene7045
Locus: gene with protein productLocation: 5q31.1

Also known as

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

Also known asCSD3 · LCD1 · CSD1 · CSD2 · BIGH3 · CDB1 · CDGG1
View full nomenclature history (9)
Previous symbolsCSD3, LCD1, CSD1, CSD2
Alias symbolsBIGH3, CDB1, CDGG1
Previous namestransforming growth factor, beta-induced, 68kD, transforming growth factor, beta-induced, 68kDa

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.

Corneal Dystrophies, Hereditary

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.