CWC22

Gene

CWC22 spliceosome associated protein

HGNCHGNC:29322 EnsemblENSG00000163510 NCBI Gene57703

Locus: gene with protein productLocation: 2q31.3

Also known as

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

Also known asKIAA1604 · EIF4GL · fSAPb · NCM

View full nomenclature history (9)

Alias symbolsKIAA1604, EIF4GL, fSAPb, NCM

Previous namesCWC22 spliceosome associated protein homolog, CWC22 spliceosome-associated protein, CWC22 homolog, spliceosome-associated protein, CWC22 spliceosome-associated protein homolog (S. cerevisiae)

Alias namesfunctional spliceosome-associated protein b

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.

Neurodegenerative Diseases

Dengue

Intelligence

Drug Hypersensitivity

Self-injurious ideation

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.

NTC associated proteinsSpliceosomal Bact complexSpliceosomal C complexSpliceosomal P complexMIF4G domain containing proteins

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2025-06-27.

Open TargetsGene–disease associations from the Open Targets Platform.