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Gene

SLC2A10

solute carrier family 2 member 10

Summary

Cytogenetic location
20q13.12
Coordinates
Chromosome 20: 46,709,649–46,736,347 (GRCh38)
Exons
5 exons across 26.7 kb
Protein
541 amino acids
Also known as
GLUT10, GLUT-10
MANE Select transcript
ENST00000359271.4NM_030777.4
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 report relevant to this gene

  • Cutis Laxa

    • Cutis laxa (CL) is an inherited or acquired connective tissue disorder characterized by wrinkled, redundant and sagging inelastic skin associated with skeletal and developmental anomalies and, in some cases, with severe systemic involvement. Several different forms of inherited CL have been described, differentiated on the basis of the mode of inheritance and differences in the extent of internal organ involvement, associated anomalies and disease severity.

      • ClinGen rates the link definitive
      • 6 GenCC submitters rate it definitive or strong

How SLC2A10 is laid out

  • Coding sequence
  • Untranslated region
  • Intron
  • Direction of transcription
  • Known disease-causing sites
  • Stretches short reads find hard
Chromosome 20, with a bracket where SLC2A10 sits. SLC2A10 and 10 genes near it on chromosome 20, from 46,222,998 to 47,222,997.Chromosome 2020q13.12p13p12.3p12.2p12.1p11.23p11.22p11.21p11.1q11.1q11.21q11.22q11.23q12q13.11q13.12q13.13q13.2q13.31q13.32q13.3346.4 Mb46.6 Mb46.8 Mb47 Mb47.2 MbCDH22: 46,173,737–46,309,009, reverse strandCDH22SLC35H1: 46,345,980–46,364,460, reverse strandSLC35H1ELMO2: 46,366,045–46,432,985, reverse strandELMO2ZNF840P: 46,459,441–46,495,558, forward strandZNF840PZNF334: 46,499,630–46,513,596, reverse strandZNF334OCSTAMP: 46,540,946–46,550,654, reverse strandOCSTAMPSLC13A3: 46,557,823–46,684,467, reverse strandSLC13A3TP53RK: 46,684,344–46,689,664, reverse strandTP53RKSLC2A10: 46,709,649–46,736,347, forward strandSLC2A10EYA2: 46,894,587–47,188,844, forward strandEYA2ZMYND8: 47,209,214–47,357,806, reverse strandZMYND8Diagram of SLC2A10: 5 exons on the forward strand of chromosome 20Exon 1: 1 known disease-causing siteExon 2: 32 known disease-causing sitesExon 3: 5 known disease-causing sitesExon 4: 3 known disease-causing sitesExon 1: 46,709,649–46,709,740, 92 basesExon 2: 46,725,041–46,726,324, 1,284 basesExon 3: 46,726,864–46,726,986, 123 basesExon 4: 46,729,353–46,729,488, 136 basesExon 5: 46,733,756–46,736,347, 2,592 bases123455′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 26.7 kb; 1,626 of those bases code for the protein.

How a genome test reads SLC2A10

46

positions in SLC2A10 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 26.7 kb of SLC2A10, 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.
  • GenCC and ClinGen, released 2026-10-16: which conditions the gene is linked to, and how strongly.
  • The ACMG secondary findings list, SF v3.2.
  • 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.). SLC2A10 gene: solute carrier family 2 member 10. Retrieved 16 October 2026, from https://dantelabs.com/genes/slc2a10

Vancouver

Dante Labs. SLC2A10 gene: solute carrier family 2 member 10 [Internet]. [cited 16 October 2026]. Available from: https://dantelabs.com/genes/slc2a10

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