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Gene

RDH11

retinol dehydrogenase 11

Summary

Cytogenetic location
14q24.1
Coordinates
Chromosome 14: 67,676,800–67,695,764 (GRCh38)
Exons
7 exons across 19 kb
Protein
318 amino acids
Also known as
MDT1, SDR7C1, ARSDR1
MANE Select transcript
ENST00000381346.9NM_016026.4
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 reports relevant to this gene

No Genome Test report reads RDH11 yet. The test sequences your whole genome, so your data includes it all the same.

How RDH11 is laid out

  • Coding sequence
  • Untranslated region
  • Intron
  • Direction of transcription
  • Known disease-causing sites
  • Stretches short reads find hard
Chromosome 14, with a bracket where RDH11 sits. RDH11 and 14 genes near it on chromosome 14, from 67,186,282 to 68,186,281.Chromosome 1414q24.1p13p12p11.2p11.1q11.1q11.2q12q13.1q13.2q13.3q21.1q21.2q21.3q22.1q22.2q22.3q23.1q23.2q23.3q24.1q24.2q24.3q31.1q31.2q31.3q32.11q32.12q32.13q32.2q32.31q32.32q32.3367.2 Mb67.4 Mb67.6 Mb67.8 Mb68 MbGARIN2: 67,189,328–67,228,550, forward strandGARIN2PALS1: 67,240,713–67,336,061, forward strandPALS1ATP6V1D: 67,294,371–67,360,265, reverse strandATP6V1DEIF2S1: 67,359,993–67,394,395, forward strandEIF2S1PLEK2: 67,385,652–67,412,236, reverse strandPLEK2TMEM229B: 67,447,084–67,533,878, reverse strandTMEM229BPLEKHH1: 67,533,063–67,589,725, forward strandPLEKHH1PIGH: 67,581,955–67,600,316, reverse strandPIGHARG2: 67,619,857–67,667,328, forward strandARG2VTI1B: 67,635,307–67,674,920, reverse strandVTI1B: 67,659,820–67,690,367, reverse strandRDH11: 67,676,800–67,695,764, reverse strandRDH11RDH12: 67,701,886–67,734,451, forward strandRDH12ZFYVE26: 67,727,374–67,816,590, reverse strandZFYVE26RAD51B: 67,819,741–68,730,218, forward strandRAD51BDiagram of RDH11: 7 exons on the reverse strand of chromosome 14Exon 6: 1 known disease-causing siteExon 3: 2 known disease-causing sitesExon 7: 67,676,800–67,678,423, 1,624 basesExon 6: 67,685,015–67,685,204, 190 basesExon 5: 67,690,212–67,690,421, 210 basesExon 4: 67,691,140–67,691,244, 105 basesExon 3: 67,692,438–67,692,593, 156 basesExon 2: 67,692,934–67,693,052, 119 basesExon 1: 67,695,630–67,695,764, 135 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 2.5 kb of the gene's 19 kb; 957 of those bases code for the protein.

How a genome test reads RDH11

3

positions in RDH11 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 19 kb of RDH11, introns included, not only the 2.5 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.). RDH11 gene: retinol dehydrogenase 11. Retrieved 16 October 2026, from https://dantelabs.com/genes/rdh11

Vancouver

Dante Labs. RDH11 gene: retinol dehydrogenase 11 [Internet]. [cited 16 October 2026]. Available from: https://dantelabs.com/genes/rdh11

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