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SCAF4

Gene

SR-related CTD associated factor 4

HGNCHGNC:19304EnsemblENSG00000156304NCBI Gene57466
Locus: gene with protein productLocation: 21q22.11

Also known as

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

Also known asSFRS15 · KIAA1172 · DKFZp434E098 · SRA4
View full nomenclature history (5)
Previous symbolsSFRS15
Alias symbolsKIAA1172, DKFZp434E098, SRA4
Previous namessplicing factor, arginine/serine-rich 15

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.

Genetic Diseases, Inborn
Complex neurodevelopmental disorder
Neurodevelopmental Disorders
Protozoan Infections

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.

RNA binding motif 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.