MNX1

Gene

motor neuron and pancreas homeobox 1

HGNCHGNC:4979 EnsemblENSG00000130675 NCBI Gene3110

Locus: gene with protein productLocation: 7q36.3

Also known as

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

Also known asHLXB9 · HB9 · HOXHB9 · SCRA1

View full nomenclature history (6)

Previous symbolsHLXB9

Alias symbolsHB9, HOXHB9, SCRA1

Previous nameshomeo box HB9, homeobox HB9

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

Permanent neonatal diabetes mellitus

Diabetes Mellitus, Type 2

Carcinoma, Non-Small-Cell Lung

Urinary bladder carcinoma

Carcinoma, Hepatocellular

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.

HOXL subclass homeoboxes

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-01-20.

Open TargetsGene–disease associations from the Open Targets Platform.