Gene
ACSL4
acyl-CoA synthetase long chain family member 4
- HGNC 3571↗(opens in a new tab)
- Ensembl gene ENSG00000068366↗(opens in a new tab)
- NCBI Gene 2182↗(opens in a new tab)
Summary
- Cytogenetic location
- Xq23
- Coordinates
- Chromosome X: 109,641,335–109,733,257 (GRCh38)
- Exons
- 16 exons across 91.9 kb
- Protein
- 670 amino acids
- Also known as
- ACS4, LACS4
- Previous symbols
- FACL4, MRX63, MRX68
- MANE Select transcript
- ENST00000672401.1NM_001318510.2
- 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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Intellectual Disability
One of 233 genes linked to it
- ClinGen rates the link definitive
- 4 GenCC submitters rate it definitive or strong
How ACSL4 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 4.9 kb of the gene's 91.9 kb; 2,013 of those bases code for the protein.
How a genome test reads ACSL4
8
positions in ACSL4 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 91.9 kb of ACSL4, introns included, not only the 4.9 kb of exons.
Genes linked to the same conditions
- ADKadenosine kinaseShares 1 condition
- ADNPactivity dependent neuroprotector homeoboxShares 1 condition
- AFF2ALF transcription elongation factor 2Shares 1 condition
- AHDC1AT-hook DNA binding motif containing 1Shares 1 condition
- ALKBH8alkB homolog 8, tRNA methyltransferaseShares 1 condition
- ANK3ankyrin 3Shares 1 condition
- ANKRD11ankyrin repeat domain 11Shares 1 condition
- AP1S2adaptor related protein complex 1 subunit sigma 2Shares 1 condition
- AP2M1adaptor related protein complex 2 subunit mu 1Shares 1 condition
- ARHGEF9Cdc42 guanine nucleotide exchange factor 9Shares 1 condition
- ARID1AAT-rich interaction domain 1AShares 1 condition
- ARID1BAT-rich interaction domain 1BShares 1 condition
Traits linked to ACSL4
The Human Phenotype Ontology lists these as features of the rare conditions ACSL4 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.). ACSL4 gene: acyl-CoA synthetase long chain family member 4. Retrieved 17 October 2026, from https://dantelabs.com/genes/acsl4
Dante Labs. ACSL4 gene: acyl-CoA synthetase long chain family member 4 [Internet]. [cited 17 October 2026]. Available from: https://dantelabs.com/genes/acsl4
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