Gene
SLC19A1
solute carrier family 19 member 1
- HGNC 10937↗(opens in a new tab)
- Ensembl gene ENSG00000173638↗(opens in a new tab)
- NCBI Gene 6573↗(opens in a new tab)
Summary
- Cytogenetic location
- 21q22.3
- Coordinates
- Chromosome 21: 45,512,565–45,542,440 (GRCh38)
- Exons
- 6 exons across 29.9 kb
- Protein
- 591 amino acids
- Also known as
- FOLT, RFC1, IFC-1, RFC, hRFC, RFT-1
- MANE Select transcript
- ENST00000311124.9NM_194255.4
- 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.
Read SLC19A1, and the rest of your genome, with one test.
From $449Free shipping · Results in 6–8 weeks
Get my Genome TestCurated reports relevant to this gene
No Genome Test report reads SLC19A1 yet. The test sequences your whole genome, so your data includes it all the same.
How SLC19A1 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 5 kb of the gene's 29.9 kb; 1,776 of those bases code for the protein.
How a genome test reads SLC19A1
1
position in SLC19A1 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 29.9 kb of SLC19A1, introns included, not only the 5 kb of exons.
Traits linked to SLC19A1
The Human Phenotype Ontology lists these as features of the rare conditions SLC19A1 can cause. Each trait's page lists the other genes linked to it.
Abnormality of blood and blood-forming tissues
- Decreased blood lymphocyte number
- Episodic hemolytic anemia
- Erythroid dysplasia
- Folate-responsive megaloblastic anemia
- Hypersegmentation of neutrophil nuclei
- Hypofibrinogenemia
- Low platelet count
- Megaloblastic anemia
Show 2 more traits
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.). SLC19A1 gene: solute carrier family 19 member 1. Retrieved 17 October 2026, from https://dantelabs.com/genes/slc19a1
Dante Labs. SLC19A1 gene: solute carrier family 19 member 1 [Internet]. [cited 17 October 2026]. Available from: https://dantelabs.com/genes/slc19a1
One test. A lifetime of answers.
From $449Free shipping · Results in 6–8 weeks