TMSB4Y

Gene

thymosin beta 4 Y-linked

HGNCHGNC:11882 EnsemblENSG00000154620 NCBI Gene9087

Locus: gene with protein productLocation: Yq11.221

Also known as

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

Also known asTB4Y

View full nomenclature history (2)

Alias symbolsTB4Y

Previous namesthymosin, beta 4, Y chromosome

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.

Familial isolated dilated cardiomyopathy

Hereditary cerebral hemorrhage with amyloidosis, Piedmont type

Hereditary cerebral hemorrhage with amyloidosis, Italian type

Hereditary cerebral hemorrhage with amyloidosis, Dutch type

Hereditary cerebral hemorrhage with amyloidosis, Iowa type

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.

Minor histocompatibility antigensThymosin beta 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.