ASCC1

Gene

activating signal cointegrator 1 complex subunit 1

HGNCHGNC:24268 EnsemblENSG00000138303 NCBI Gene51008

Locus: gene with protein productLocation: 10q22.1

Also known as

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

Also known asCGI-18 · ASC1p50 · Em:AC022392.3 · p50

View full nomenclature history (4)

Alias symbolsCGI-18, ASC1p50, Em:AC022392.3, p50

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.

Proximal spinal muscular atrophy

Muscular Atrophy, Spinal

Barrett Esophagus

Genetic Diseases, Inborn

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.

Activating signal cointegrator 1 complex

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-01-20.

Open TargetsGene–disease associations from the Open Targets Platform.