Gene
SLC51A
solute carrier family 51 member A
- HGNC 29955↗(opens in a new tab)
- Ensembl gene ENSG00000163959↗(opens in a new tab)
- NCBI Gene 200931↗(opens in a new tab)
Summary
- Cytogenetic location
- 3q29
- Coordinates
- Chromosome 3: 196,216,534–196,233,427 (GRCh38)
- Exons
- 9 exons across 16.9 kb
- Protein
- 340 amino acids
- Also known as
- OSTalpha, SLC51A1
- MANE Select transcript
- ENST00000296327.10NM_152672.6
- 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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How SLC51A 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 1.4 kb of the gene's 16.9 kb; 1,023 of those bases code for the protein.
Traits linked to SLC51A
The Human Phenotype Ontology lists these as features of the rare conditions SLC51A 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.
- The Human Phenotype Ontology, release 2026-09-01: the traits linked to the gene. Find out more at hpo.jax.org.
Cite this page
Dante Labs. (n.d.). SLC51A gene: solute carrier family 51 member A. Retrieved 17 October 2026, from https://dantelabs.com/genes/slc51a
Dante Labs. SLC51A gene: solute carrier family 51 member A [Internet]. [cited 17 October 2026]. Available from: https://dantelabs.com/genes/slc51a
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