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TBC1D32

Gene

TBC1 domain family member 32

HGNCHGNC:21485EnsemblENSG00000146350NCBI Gene221322
Locus: gene with protein productLocation: 6q22.31

Also known as

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

Also known asC6orf171 · C6orf170 · FLJ30899 · dJ310J6.1 · FLJ34235 · bA57L9.1 · BROMI
View full nomenclature history (11)
Previous symbolsC6orf171, C6orf170
Alias symbolsFLJ30899, dJ310J6.1, FLJ34235, bA57L9.1, BROMI
Previous nameschromosome 6 open reading frame 171, chromosome 6 open reading frame 170, TBC1 domain family, member 32
Alias namesbroad-minded homolog

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.

Ciliopathy
Retinitis Pigmentosa
Atrial Fibrillation
Hypopituitarism
Genetic Diseases, Inborn
Neurodegenerative Diseases

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.

Armadillo like helical domain containing

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-06-16.
Open TargetsGene–disease associations from the Open Targets Platform.