Gene
MNX1
motor neuron and pancreas homeobox 1
- HGNC 4979↗(opens in a new tab)
- Ensembl gene ENSG00000130675↗(opens in a new tab)
- NCBI Gene 3110↗(opens in a new tab)
Summary
- Cytogenetic location
- 7q36.3
- Coordinates
- Chromosome 7: 157,004,854–157,010,663 (GRCh38)
- Exons
- 3 exons across 5.8 kb
- Protein
- 401 amino acids
- Also known as
- HB9, HOXHB9, SCRA1
- Previous symbols
- HLXB9
- MANE Select transcript
- ENST00000252971.11NM_005515.4
- Locus type
- gene with protein product
- Very high
- Confident
- Low
- Very low
Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
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Get my Genome TestCurated reports relevant to this gene
Diabetes Mellitus
A metabolic disorder characterized by abnormally high blood sugar levels due to diminished production of insulin or insulin resistance/desensitization.
- 2 GenCC submitters rate it definitive or strong
What knowing changes
Teplizumab (Tzield) for stage 2 presymptomatic T1D (FDA approved 2022); insulin replacement at clinical T1D onset; TrialNet autoantibody screening for high-risk relatives; closed-loop insulin delivery systems
Neonatal Diabetes Mellitus
Diabetes diagnosed in the first months of life, either permanent or transient, caused by single-gene defects in insulin production or secretion.
- 2 GenCC submitters rate it definitive or strong
What knowing changes
Most people with KCNJ11 or ABCC8 neonatal diabetes can switch from insulin injections to sulfonylurea tablets, often with better glucose control.
How MNX1 is laid out
- Coding sequence
- Untranslated region
- Intron
- Direction of transcription
- Known disease-causing sites
Exons of the gene's MANE Select transcript (release v1.5), from NCBI and EMBL-EBI, on the GRCh38 reference genome.
Chromosome bands from UCSC's GRCh38 ideogram (2022-10-29).
Nearby genes from Ensembl release 116, on GRCh38.
Exons make up 2.2 kb of the gene's 5.8 kb; 1,206 of those bases code for the protein.
How a genome test reads MNX1
12
positions in MNX1 where ClinVar classes a change as pathogenic or likely pathogenic
None of them falls in a region short reads find hard.
A whole genome covers all 5.8 kb of MNX1, introns included, not only the 2.2 kb of exons.
Genes linked to the same conditions
- ABCC8ATP binding cassette subfamily C member 8Shares 2 conditions
- BSCL2BSCL2 lipid droplet biogenesis associated, seipinShares 2 conditions
- EIF2B1eukaryotic translation initiation factor 2B subunit alphaShares 2 conditions
- GATA4GATA binding protein 4Shares 2 conditions
- GATA6GATA binding protein 6Shares 2 conditions
- GCKglucokinaseShares 2 conditions
- GLIS3GLIS family zinc finger 3Shares 2 conditions
- HNF1BHNF1 homeobox BShares 2 conditions
- IL2RAinterleukin 2 receptor subunit alphaShares 2 conditions
- INSinsulinShares 2 conditions
- KCNJ11potassium inwardly rectifying channel subfamily J member 11Shares 2 conditions
- NEUROD1neuronal differentiation 1Shares 2 conditions
Traits linked to MNX1
The Human Phenotype Ontology lists these as features of the rare conditions MNX1 can cause. Each trait's page lists the other genes linked to it.
External links
Gene records
Transcript
Protein
Where this comes from
- HGNC: the gene's symbol, name, other symbols and location.
- MANE Select v1.5, from NCBI and EMBL-EBI: the transcript, its exons and coding sequence.
- GenCC and ClinGen, released 2026-10-16: which conditions the gene is linked to, and how strongly.
- The ACMG secondary findings list, SF v3.2.
- ClinVar and the GIAB stratifications: known disease-causing sites, and the regions short reads find hard.
- The Human Phenotype Ontology, release 2026-09-01: the traits linked to the gene. Find out more at hpo.jax.org.
- Data release 2026.10.16-c6eea6bf.
Cite this page
Dante Labs. (n.d.). MNX1 gene: motor neuron and pancreas homeobox 1. Retrieved 16 October 2026, from https://dantelabs.com/genes/mnx1
Dante Labs. MNX1 gene: motor neuron and pancreas homeobox 1 [Internet]. [cited 16 October 2026]. Available from: https://dantelabs.com/genes/mnx1
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