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MBNL1

Gene

muscleblind like splicing regulator 1

HGNCHGNC:6923EnsemblENSG00000152601NCBI Gene4154
Locus: gene with protein productLocation: 3q25.1-q25.2

Also known as

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

Also known asMBNL · KIAA0428 · EXP42 · EXP40 · EXP35 · EXP
View full nomenclature history (9)
Previous symbolsMBNL
Alias symbolsKIAA0428, EXP42, EXP40, EXP35, EXP
Previous namesmuscleblind (Drosophila)-like, muscleblind-like (Drosophila), muscleblind-like splicing regulator 1

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.

Diabetes Mellitus, Type 2
Diabetes Mellitus
Prostate carcinoma
Alopecia
Alcohol drinking
Myotonic Dystrophy

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.

Zinc fingers CCCH-typeMuscleblind like splicing regulator family

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-01-20.
Open TargetsGene–disease associations from the Open Targets Platform.