ASB10

Gene

ankyrin repeat and SOCS box containing 10

HGNCHGNC:17185 EnsemblENSG00000146926 NCBI Gene136371

Locus: gene with protein productLocation: 7q36.1

Also known as

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

Also known asGLC1F

View full nomenclature history (3)

Previous symbolsGLC1F

Previous namesankyrin repeat and SOCS box-containing 10, glaucoma 1, open angle, F (adult-onset)

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.

Glaucoma, Open-Angle

Acquired Hyperostosis Syndrome

Cardiomegaly

Autosomal dominant secondary polycythemia

Glaucoma

Erythrocytosis, familial, 4

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.

Ankyrin repeat 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.