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DDX41

Gene

DEAD-box helicase 41

HGNCHGNC:18674EnsemblENSG00000183258NCBI Gene51428
Locus: gene with protein productLocation: 5q35.3

Also known as

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

Also known asABS · MGC8828
View full nomenclature history (4)
Alias symbolsABS, MGC8828
Previous namesDEAD (Asp-Glu-Ala-Asp) box polypeptide 41
Alias namesAbstrakt

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.

Leukemia, Myeloid, Acute
Myelodysplastic syndrome
Leukemia, Myeloid
Genetic Diseases, Inborn
Neurodegenerative Diseases
chronic myelogenous leukemia, BCR-ABL1 positive

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.

DEAD-box helicasesSpliceosomal C complexSpliceosomal P complex

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-10-25.
Open TargetsGene–disease associations from the Open Targets Platform.