Skip to content
Use your HSA or FSA funds

Gene

MED17

mediator complex subunit 17

Summary

Cytogenetic location
11q21
Coordinates
Chromosome 11: 93,784,282–93,814,963 (GRCh38)
Exons
12 exons across 30.7 kb
Protein
651 amino acids
Also known as
CRSP77, TRAP80, DRIP80, SRB4
Previous symbols
CRSP6
MANE Select transcript
ENST00000251871.9NM_004268.5
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 MED17 yet. The test sequences your whole genome, so your data includes it all the same.

How MED17 is laid out

  • Coding sequence
  • Untranslated region
  • Intron
  • Direction of transcription
  • Known disease-causing sites
  • Stretches short reads find hard
Chromosome 11, with a bracket where MED17 sits. MED17 and 9 genes near it on chromosome 11, from 93,299,623 to 94,299,622.Chromosome 1111q21p15.5p15.4p15.3p15.2p15.1p14.3p14.2p14.1p13p12p11.2p11.12p11.11q11q12.1q12.2q12.3q13.1q13.2q13.3q13.4q13.5q14.1q14.2q14.3q21q22.1q22.2q22.3q23.1q23.2q23.3q24.1q24.2q24.3q2593.4 Mb93.6 Mb93.8 Mb94 Mb94.2 MbDEUP1: 93,329,971–93,438,487, forward strandDEUP1SMCO4: 93,478,468–93,543,764, reverse strandSMCO4CEP295: 93,661,642–93,730,358, forward strandCEP295TAF1D: 93,729,948–93,784,391, reverse strandTAF1DBKGD: 93,741,566–93,770,084, forward strandBKGD: 93,741,664–93,812,378, forward strandMED17: 93,784,282–93,814,963, forward strandMED17VSTM5: 93,818,232–93,850,641, reverse strandVSTM5HEPHL1: 94,021,354–94,114,208, forward strandHEPHL1PANX1: 94,128,828–94,185,019, forward strandPANX1Diagram of MED17: 12 exons on the forward strand of chromosome 11Exon 1: 4 known disease-causing sitesExon 2: 2 known disease-causing sitesExon 3: 7 known disease-causing sitesExon 4: 3 known disease-causing sitesExon 5: 1 known disease-causing siteExon 6: 4 known disease-causing sitesExon 7: 1 known disease-causing siteExon 8: 1 known disease-causing siteExon 9: 5 known disease-causing sitesExon 10: 2 known disease-causing sitesExon 11: 3 known disease-causing sitesExon 1: 93,784,282–93,784,763, 482 basesExon 2: 93,788,001–93,788,167, 167 basesExon 3: 93,790,574–93,790,793, 220 basesExon 4: 93,793,728–93,793,864, 137 basesExon 5: 93,793,951–93,794,035, 85 basesExon 6: 93,794,908–93,795,060, 153 basesExon 7: 93,796,410–93,796,540, 131 basesExon 8: 93,797,535–93,797,719, 185 basesExon 9: 93,801,835–93,801,972, 138 basesExon 10: 93,807,518–93,807,635, 118 basesExon 11: 93,809,717–93,809,876, 160 basesExon 12: 93,811,853–93,814,963, 3,111 bases1246810125′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 5.1 kb of the gene's 30.7 kb; 1,956 of those bases code for the protein.

How a genome test reads MED17

40

positions in MED17 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 30.7 kb of MED17, introns included, not only the 5.1 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.). MED17 gene: mediator complex subunit 17. Retrieved 16 October 2026, from https://dantelabs.com/genes/med17

Vancouver

Dante Labs. MED17 gene: mediator complex subunit 17 [Internet]. [cited 16 October 2026]. Available from: https://dantelabs.com/genes/med17

One test. A lifetime of answers.

From $449Free shipping · Results in 6–8 weeks

Get my Genome Test