MLXIPL

Gene

MLX interacting protein like

HGNCHGNC:12744 EnsemblENSG00000009950 NCBI Gene51085

Locus: gene with protein productLocation: 7q11.23

Also known as

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

Also known asWBSCR14 · WS-bHLH · MIO · CHREBP · MONDOB · bHLHd14

View full nomenclature history (9)

Previous symbolsWBSCR14

Alias symbolsWS-bHLH, MIO, CHREBP, MONDOB, bHLHd14

Previous namesWilliams Beuren syndrome chromosome region 14, MLX interacting protein-like

Alias namescarbohydrate response element binding protein

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.

Gout

Hyperlipidemias

Familial lipoprotein lipase deficiency

Diabetes Mellitus

Metabolic Diseases

Alcohol drinking

Diabetes Mellitus, Type 2

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.

Basic helix-loop-helix proteins

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-03-15.

Open TargetsGene–disease associations from the Open Targets Platform.