C16orf86

Gene

chromosome 16 open reading frame 86

HGNCHGNC:33755 EnsemblENSG00000159761 NCBI Gene388284

Locus: gene with protein productLocation: 16q22.1

Also known as

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

Also known asFLJ41802

View full nomenclature history (1)

Alias symbolsFLJ41802

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.

Autosomal dominant macrothrombocytopenia

Thrombocytopenia 4

Purpura, Thrombocytopenic, Idiopathic

Rare hemorrhagic disorder due to a constitutional platelet anomaly

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 2023-01-20.

Open TargetsGene–disease associations from the Open Targets Platform.