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Gene

SLC25A32

solute carrier family 25 member 32

Summary

Cytogenetic location
8q22.3
Coordinates
Chromosome 8: 103,398,638–103,415,107 (GRCh38)
Exons
7 exons across 16.5 kb
Protein
315 amino acids
Also known as
MFTC
MANE Select transcript
ENST00000297578.9NM_030780.5
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 SLC25A32 yet. The test sequences your whole genome, so your data includes it all the same.

How SLC25A32 is laid out

  • Coding sequence
  • Untranslated region
  • Intron
  • Direction of transcription
  • Known disease-causing sites
  • Stretches short reads find hard
Chromosome 8, with a bracket where SLC25A32 sits. SLC25A32 and 7 genes near it on chromosome 8, from 102,906,873 to 103,906,872.Chromosome 88q22.3p23.3p23.2p23.1p22p21.3p21.2p21.1p12p11.23p11.22p11.21p11.1q11.1q11.21q11.22q11.23q12.1q12.2q12.3q13.1q13.2q13.3q21.11q21.12q21.13q21.2q21.3q22.1q22.2q22.3q23.1q23.2q23.3q24.11q24.12q24.13q24.21q24.22q24.23q24.3103 Mb103.2 Mb103.4 Mb103.6 Mb103.8 MbATP6V1C1: 103,021,050–103,073,683, forward strandATP6V1C1BAALC: 103,140,370–103,248,401, forward strandBAALCFZD6: 103,298,433–103,332,866, forward strandFZD6CTHRC1: 103,371,497–103,383,815, forward strandCTHRC1SLC25A32: 103,398,638–103,415,107, reverse strandSLC25A32: 103,398,658–103,501,895, reverse strandDCAF13: 103,414,651–103,443,845, forward strandDCAF13RIMS2: 103,499,638–104,254,698, forward strandRIMS2Diagram of SLC25A32: 7 exons on the reverse strand of chromosome 8Exon 4: 1 known disease-causing siteExon 7: 103,398,638–103,400,546, 1,909 basesExon 6: 103,401,516–103,401,661, 146 basesExon 5: 103,401,941–103,402,054, 114 basesExon 4: 103,403,164–103,403,324, 161 basesExon 3: 103,404,776–103,404,861, 86 basesExon 2: 103,407,634–103,407,784, 151 basesExon 1: 103,414,784–103,415,107, 324 bases76543215′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 2.9 kb of the gene's 16.5 kb; 948 of those bases code for the protein.

How a genome test reads SLC25A32

1

position in SLC25A32 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 16.5 kb of SLC25A32, introns included, not only the 2.9 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.). SLC25A32 gene: solute carrier family 25 member 32. Retrieved 17 October 2026, from https://dantelabs.com/genes/slc25a32

Vancouver

Dante Labs. SLC25A32 gene: solute carrier family 25 member 32 [Internet]. [cited 17 October 2026]. Available from: https://dantelabs.com/genes/slc25a32

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