Gene
MYL9
myosin light chain 9
- HGNC 15754↗(opens in a new tab)
- Ensembl gene ENSG00000101335↗(opens in a new tab)
- NCBI Gene 10398↗(opens in a new tab)
Summary
- Cytogenetic location
- 20q11.23
- Coordinates
- Chromosome 20: 36,541,519–36,551,447 (GRCh38)
- Exons
- 4 exons across 9.9 kb
- Protein
- 172 amino acids
- Also known as
- MYRL2, MLC2, LC20, MRLC1
- MANE Select transcript
- ENST00000279022.7NM_006097.5
- 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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Hereditary Visceral Myopathy, CIPO & MMIHS
- Megacystis-microcolon-intestinal hypoperistalsis syndrome (MMIHS)
A severe newborn condition with a greatly enlarged bladder, a small colon and poor bowel movement, caused by variants in smooth-muscle genes such as ACTG2, MYH11, MYLK, MYL9 and LMOD1.
- 3 GenCC submitters rate it definitive or strong
What knowing changes
Early diagnosis supports planning for nutritional support, bladder drainage and, in some cases, transplant.
How MYL9 is laid out
- Coding sequence
- Untranslated region
- Intron
- Direction of transcription
- 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 2.8 kb of the gene's 9.9 kb; 519 of those bases code for the protein.
Genes linked to the same conditions
Traits linked to MYL9
The Human Phenotype Ontology lists these as features of the rare conditions MYL9 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.
- 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.). MYL9 gene: myosin light chain 9. Retrieved 17 October 2026, from https://dantelabs.com/genes/myl9
Dante Labs. MYL9 gene: myosin light chain 9 [Internet]. [cited 17 October 2026]. Available from: https://dantelabs.com/genes/myl9
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