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TSC22D1

Gene

TSC22 domain family member 1

HGNCHGNC:16826EnsemblENSG00000102804NCBI Gene8848
Locus: gene with protein productLocation: 13q14.11

Also known as

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

Also known asTGFB1I4 · TSC22 · MGC17597
View full nomenclature history (5)
Previous symbolsTGFB1I4
Alias symbolsTSC22, MGC17597
Previous namestransforming growth factor beta 1 induced transcript 4, TSC22 domain family, member 1

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.

Neurodegenerative Diseases
Psoriasis
Bacteremia
Amblyopia
Stroke
Alcohol drinking

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.

Gene family

HGNC gene-group membership.

TSC22 domain family

Provenance

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