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TRIOBP

Gene

TRIO and F-actin binding protein

HGNCHGNC:17009EnsemblENSG00000100106NCBI Gene11078
Locus: gene with protein productLocation: 22q13.1

Also known as

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

Also known asDFNB28 · HRIHFB2122 · KIAA1662 · Tara · TAP68
View full nomenclature history (5)
Previous symbolsDFNB28
Alias symbolsHRIHFB2122, KIAA1662, Tara, TAP68

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.

Hearing loss, autosomal recessive
Hearing Loss
Deafness
Nonsyndromic genetic hearing loss
Presbycusis
Alzheimer's Disease
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.

Pleckstrin homology domain containing

Provenance

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