HSPA12B

Gene

heat shock protein family A (Hsp70) member 12B

HGNCHGNC:16193 EnsemblENSG00000132622 NCBI Gene116835

Locus: gene with protein productLocation: 20p13

Also known as

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

Also known asC20orf60 · dJ1009E24.2

View full nomenclature history (4)

Previous symbolsC20orf60

Alias symbolsdJ1009E24.2

Previous nameschromosome 20 open reading frame 60, heat shock 70kD protein 12B

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

Myocardial Infarction

Stroke

Lymphoma, Non-Hodgkin's

Metabolic Syndrome

Sarcopenia

Drug Hypersensitivity

Myelodysplastic syndrome

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.

Heat shock 70kDa proteins

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-01-20.

Open TargetsGene–disease associations from the Open Targets Platform.