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Gene

SLC25A10

solute carrier family 25 member 10

Summary

Cytogenetic location
17q25.3
Coordinates
Chromosome 17: 81,712,284–81,721,012 (GRCh38)
Exons
11 exons across 8.7 kb
Protein
287 amino acids
Previous symbols
DIC
MANE Select transcript
ENST00000350690.10NM_012140.5
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 SLC25A10 yet. The test sequences your whole genome, so your data includes it all the same.

How SLC25A10 is laid out

  • Coding sequence
  • Untranslated region
  • Intron
  • Direction of transcription
  • Known disease-causing sites
  • Stretches short reads find hard
Chromosome 17, with a bracket where SLC25A10 sits. SLC25A10 and 41 genes near it on chromosome 17, from 81,216,648 to 82,216,647.Chromosome 1717q25.3p13.3p13.2p13.1p12p11.2p11.1q11.1q11.2q12q21.1q21.2q21.31q21.32q21.33q22q23.1q23.2q23.3q24.1q24.2q24.3q25.1q25.2q25.381.4 Mb81.6 Mb81.8 Mb82 Mb82.2 MbCEP131: 81,189,583–81,223,014, reverse strandCEP131TEPSIN: 81,228,277–81,239,095, reverse strandTEPSINNDUFAF8: 81,239,305–81,241,310, forward strandNDUFAF8SLC38A10: 81,244,811–81,295,567, reverse strandSLC38A10BAHCC1: 81,395,450–81,466,331, forward strandBAHCC1ACTG1: 81,509,413–81,523,847, reverse strandACTG1FSCN2: 81,528,372–81,542,415, forward strandFSCN2FAAP100: 81,539,885–81,553,961, reverse strandFAAP100NPLOC4: 81,556,887–81,648,465, reverse strandNPLOC4TSPAN10: 81,637,171–81,648,754, forward strandPDE6G: 81,650,459–81,663,112, reverse strandOXLD1: 81,665,033–81,666,635, reverse strandCCDC137: 81,666,698–81,673,904, forward strandARL16: 81,681,160–81,683,797, reverse strandHGS: 81,683,326–81,703,138, forward strandHGSMRPL12: 81,703,357–81,711,112, forward strandMRPL12: 81,703,371–81,720,539, forward strandSLC25A10: 81,712,284–81,721,012, forward strandSLC25A10GCGR: 81,803,105–81,814,023, forward strandGCGRMCRIP1: 81,821,790–81,833,302, reverse strandMCRIP1PPP1R27: 81,833,488–81,835,056, reverse strandPPP1R27P4HB: 81,843,158–81,860,856, reverse strandP4HBARHGDIA: 81,867,719–81,871,378, reverse strandARHGDIAALYREF: 81,887,830–81,891,835, reverse strandALYREFANAPC11: 81,890,669–81,900,991, forward strandNPB: 81,900,745–81,902,905, forward strandNPBPCYT2: 81,900,958–81,911,507, reverse strandSIRT7: 81,911,939–81,921,323, reverse strandMAFG: 81,918,270–81,927,769, reverse strandPYCR1: 81,932,378–81,942,412, reverse strandPYCR1MYADML2: 81,939,645–81,947,233, reverse strandNOTUM: 81,952,507–81,963,328, reverse strandNOTUMASPSCR1: 81,976,807–82,018,698, forward strandASPSCR1CENPX: 82,018,590–82,024,107, reverse strandCENPXLRRC45: 82,023,269–82,031,153, forward strandLRRC45RAC3: 82,031,192–82,034,218, forward strandRAC3DCXR: 82,035,136–82,037,777, reverse strandRFNG: 82,047,902–82,051,871, reverse strandGPS1: 82,050,691–82,058,063, forward strandDUS1L: 82,057,506–82,066,206, reverse strandFASN: 82,076,900–82,098,294, reverse strandFASNCCDC57: 82,101,458–82,212,885, reverse strandCCDC57Diagram of SLC25A10: 11 exons on the forward strand of chromosome 17Exon 3: 1 known disease-causing siteExon 7: 1 known disease-causing siteExon 1: 81,712,284–81,712,519, 236 basesExon 2: 81,714,953–81,715,072, 120 basesExon 3: 81,715,478–81,715,592, 115 basesExon 4: 81,715,693–81,715,741, 49 basesExon 5: 81,716,009–81,716,050, 42 basesExon 6: 81,716,812–81,716,855, 44 basesExon 7: 81,717,002–81,717,072, 71 basesExon 8: 81,717,399–81,717,491, 93 basesExon 9: 81,717,784–81,717,861, 78 basesExon 10: 81,719,831–81,719,887, 57 basesExon 11: 81,719,976–81,721,012, 1,037 bases12345678910115′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 1.9 kb of the gene's 8.7 kb; 864 of those bases code for the protein.

How a genome test reads SLC25A10

3

positions in SLC25A10 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 8.7 kb of SLC25A10, introns included, not only the 1.9 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.). SLC25A10 gene: solute carrier family 25 member 10. Retrieved 17 October 2026, from https://dantelabs.com/genes/slc25a10

Vancouver

Dante Labs. SLC25A10 gene: solute carrier family 25 member 10 [Internet]. [cited 17 October 2026]. Available from: https://dantelabs.com/genes/slc25a10

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