TIMCC

Gene

TIM double twin CX3C motif chaperone

HGNCHGNC:25911 EnsemblENSG00000035141 NCBI Gene84908

Locus: gene with protein productLocation: 2p13.3

Also known as

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

Also known asFAM136A · FLJ14668

View full nomenclature history (4)

Previous symbolsFAM136A

Alias symbolsFLJ14668

Previous namesfamily with sequence similarity 136 member A

Alias nameshypothetical protein FLJ14668

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.

Meniere's Disease

Osteoarthritis, Hip

Frontotemporal Dementia

Ovarian dysfunction

Poisoning

Response to antihypertensive drug

Hearing loss, autosomal recessive

Deafness

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.

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2026-01-05.

Open TargetsGene–disease associations from the Open Targets Platform.