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Gene

SLC26A11

solute carrier family 26 member 11

Summary

Cytogenetic location
17q25.3
Coordinates
Chromosome 17: 80,220,427–80,253,500 (GRCh38)
Exons
18 exons across 33.1 kb
Protein
606 amino acids
MANE Select transcript
ENST00000361193.8NM_001166347.2
Locus type
gene with protein product

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 SLC26A11 yet. The test sequences your whole genome, so your data includes it all the same.

How SLC26A11 is laid out

  • Coding sequence
  • Untranslated region
  • Intron
  • Direction of transcription
  • Stretches short reads find hard
Chromosome 17, with a bracket where SLC26A11 sits. SLC26A11 and 15 genes near it on chromosome 17, from 79,736,964 to 80,736,963.Chromosome 1717q25.3p13.3p13.2p13.1p12p11.2p11.1q11.1q11.2q12q21.1q21.2q21.31q21.32q21.33q22q23.1q23.2q23.3q24.1q24.2q24.3q25.1q25.2q25.379.8 Mb80 Mb80.2 Mb80.4 Mb80.6 MbENPP7: 79,728,809–79,742,930, forward strandENPP7CBX2: 79,778,135–79,788,394, forward strandCBX2CBX8: 79,792,132–79,801,683, reverse strandCBX8CBX4: 79,833,156–79,839,486, reverse strandCBX4TBC1D16: 79,932,343–80,035,887, reverse strandTBC1D16CCDC40: 80,036,000–80,100,613, forward strandCCDC40GAA: 80,101,526–80,119,881, forward strandGAAEIF4A3: 80,132,700–80,147,151, reverse strandEIF4A3CARD14: 80,169,992–80,216,073, forward strandCARD14SGSH: 80,206,716–80,220,928, reverse strandSGSHSLC26A11: 80,220,427–80,253,500, forward strandSLC26A11RNF213: 80,260,807–80,398,794, forward strandRNF213ENDOV: 80,415,147–80,438,086, forward strandENDOVNPTX1: 80,466,834–80,477,843, reverse strandNPTX1RPTOR: 80,544,819–80,966,371, forward strandRPTOR: 80,545,075–80,545,134, forward strandDiagram of SLC26A11: 18 exons on the forward strand of chromosome 17Exon 1: 80,220,427–80,220,496, 70 basesExon 2: 80,220,916–80,221,115, 200 basesExon 3: 80,221,548–80,221,794, 247 basesExon 4: 80,222,655–80,222,847, 193 basesExon 5: 80,223,252–80,223,337, 86 basesExon 6: 80,225,837–80,225,916, 80 basesExon 7: 80,227,818–80,227,960, 143 basesExon 8: 80,236,928–80,237,103, 176 basesExon 9: 80,237,522–80,237,594, 73 basesExon 10: 80,241,771–80,241,821, 51 basesExon 11: 80,245,196–80,245,256, 61 basesExon 12: 80,246,154–80,246,209, 56 basesExon 13: 80,246,509–80,246,649, 141 basesExon 14: 80,248,130–80,248,257, 128 basesExon 15: 80,248,575–80,248,674, 100 basesExon 16: 80,249,154–80,249,287, 134 basesExon 17: 80,251,329–80,251,401, 73 basesExon 18: 80,252,625–80,253,500, 876 bases1246810121416185′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 33.1 kb; 1,821 of those bases code for the protein.

How a genome test reads SLC26A11

1

position in SLC26A11 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 33.1 kb of SLC26A11, 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.
  • Data release 2026.10.16-c6eea6bf.

Cite this page

APA

Dante Labs. (n.d.). SLC26A11 gene: solute carrier family 26 member 11. Retrieved 17 October 2026, from https://dantelabs.com/genes/slc26a11

Vancouver

Dante Labs. SLC26A11 gene: solute carrier family 26 member 11 [Internet]. [cited 17 October 2026]. Available from: https://dantelabs.com/genes/slc26a11

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