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Gene

SLC25A24

solute carrier family 25 member 24

Summary

Cytogenetic location
1p13.3
Coordinates
Chromosome 1: 108,134,043–108,200,343 (GRCh38)
Exons
10 exons across 66.3 kb
Protein
477 amino acids
Also known as
DKFZp586G0123, APC1, SCAMC1, SCAMC-1
MANE Select transcript
ENST00000565488.6NM_013386.5
Locus type
gene with protein product
  • Very high
  • Confident
  • Low
  • Very low

Reference genomeGRCh38

Positions on gene and variant pages follow this choice, in this browser.

Curated reports relevant to this gene

No Genome Test report reads SLC25A24 yet. The test sequences your whole genome, so your data includes it all the same.

How SLC25A24 is laid out

  • Coding sequence
  • Untranslated region
  • Intron
  • Direction of transcription
  • Known disease-causing sites
  • Stretches short reads find hard
Chromosome 1, with a bracket where SLC25A24 sits. SLC25A24 and 5 genes near it on chromosome 1, from 107,667,193 to 108,667,192.Chromosome 11p13.3p36.33p36.32p36.31p36.23p36.22p36.21p36.13p36.12p36.11p35.3p35.2p35.1p34.3p34.2p34.1p33p32.3p32.2p32.1p31.3p31.2p31.1p22.3p22.2p22.1p21.3p21.2p21.1p13.3p13.2p13.1p12p11.2p11.1q11q12q21.1q21.2q21.3q22q23.1q23.2q23.3q24.1q24.2q24.3q25.1q25.2q25.3q31.1q31.2q31.3q32.1q32.2q32.3q41q42.11q42.12q42.13q42.2q42.3q43q44107.8 Mb108 Mb108.2 Mb108.4 Mb108.6 MbVAV3: 107,571,161–107,965,275, reverse strandVAV3SLC25A24: 108,134,043–108,200,343, reverse strandSLC25A24NBPF4: 108,222,464–108,244,081, reverse strandNBPF4NBPF6: 108,450,282–108,471,920, forward strandNBPF6EEIG2: 108,560,031–108,644,900, forward strandEEIG2HENMT1: 108,648,285–108,661,526, reverse strandHENMT1Diagram of SLC25A24: 10 exons on the reverse strand of chromosome 1Exon 5: 2 known disease-causing sitesExon 10: 108,134,043–108,136,837, 2,795 basesExon 9: 108,139,058–108,139,208, 151 basesExon 8: 108,143,543–108,143,710, 168 basesExon 7: 108,148,279–108,148,386, 108 basesExon 6: 108,154,983–108,155,135, 153 basesExon 5: 108,157,462–108,157,620, 159 basesExon 4: 108,161,182–108,161,293, 112 basesExon 3: 108,181,941–108,182,028, 88 basesExon 2: 108,185,828–108,185,954, 127 basesExon 1: 108,199,956–108,200,343, 388 bases109876543215′3′

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 4.2 kb of the gene's 66.3 kb; 1,434 of those bases code for the protein.

How a genome test reads SLC25A24

2

positions in SLC25A24 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 66.3 kb of SLC25A24, introns included, not only the 4.2 kb of exons.

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

APA

Dante Labs. (n.d.). SLC25A24 gene: solute carrier family 25 member 24. Retrieved 17 October 2026, from https://dantelabs.com/genes/slc25a24

Vancouver

Dante Labs. SLC25A24 gene: solute carrier family 25 member 24 [Internet]. [cited 17 October 2026]. Available from: https://dantelabs.com/genes/slc25a24

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