Gene
MEOX1
mesenchyme homeobox 1
- HGNC 7013↗(opens in a new tab)
- Ensembl gene ENSG00000005102↗(opens in a new tab)
- NCBI Gene 4222↗(opens in a new tab)
Summary
- Cytogenetic location
- 17q21.31
- Coordinates
- Chromosome 17: 43,640,389–43,661,922 (GRCh38)
- Exons
- 3 exons across 21.5 kb
- Protein
- 254 amino acids
- Also known as
- MOX1
- MANE Select transcript
- ENST00000318579.9NM_004527.4
- 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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No Genome Test report reads MEOX1 yet. The test sequences your whole genome, so your data includes it all the same.
How MEOX1 is laid out
- Coding sequence
- Untranslated region
- Intron
- Direction of transcription
- Known disease-causing sites
- Stretches short reads find hard
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 2.7 kb of the gene's 21.5 kb; 765 of those bases code for the protein.
How a genome test reads MEOX1
5
positions in MEOX1 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 21.5 kb of MEOX1, introns included, not only the 2.7 kb of exons.
Traits linked to MEOX1
The Human Phenotype Ontology lists these as features of the rare conditions MEOX1 can cause. Each trait's page lists the other genes linked to it.
Abnormality of the musculoskeletal system
- Abnormal vertebral segmentation and fusion
- Abnormality of the vertebral column
- Cervical C2/C3 vertebral fusion
- Abnormality of the ribs
- Abnormality of the shoulder
- High shoulder blade
- Scoliosis
- Abnormal sacrum morphology
Show 2 more traits
Abnormality of head or neck
- Facial asymmetry
- Limitation of neck motion
- Low hairline at back of neck
- Short neck
- Webbed neck
- Congenital muscular torticollis
- Cleft palate
- Cleft upper lip
Show 1 more trait
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.
- 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.). MEOX1 gene: mesenchyme homeobox 1. Retrieved 16 October 2026, from https://dantelabs.com/genes/meox1
Dante Labs. MEOX1 gene: mesenchyme homeobox 1 [Internet]. [cited 16 October 2026]. Available from: https://dantelabs.com/genes/meox1
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