Skip to content
Use your HSA or FSA funds

Gene

TRIM37

tripartite motif containing 37

Summary

Cytogenetic location
17q22
Coordinates
Chromosome 17: 58,998,202–59,106,880 (GRCh38)
Exons
24 exons across 108.7 kb
Protein
964 amino acids
Also known as
KIAA0898, POB1, TEF3
Previous symbols
MUL
MANE Select transcript
ENST00000262294.12NM_015294.6
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 TRIM37 yet. The test sequences your whole genome, so your data includes it all the same.

How TRIM37 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 TRIM37 sits. TRIM37 and 10 genes near it on chromosome 17, from 58,552,541 to 59,552,540.Chromosome 1717q22p13.3p13.2p13.1p12p11.2p11.1q11.1q11.2q12q21.1q21.2q21.31q21.32q21.33q22q23.1q23.2q23.3q24.1q24.2q24.3q25.1q25.2q25.358.6 Mb58.8 Mb59 Mb59.2 Mb59.4 MbTEX14: 58,556,678–58,692,055, reverse strandTEX14IGBP1C: 58,660,424–58,692,055, reverse strandIGBP1CRAD51C: 58,692,569–58,735,611, forward strandRAD51CPPM1E: 58,755,851–58,985,179, forward strandPPM1ETRIM37: 58,998,202–59,106,880, reverse strandTRIM37SKA2: 59,109,857–59,155,260, reverse strandSKA2PRR11: 59,155,732–59,206,709, forward strandPRR11: 59,197,566–59,215,226, forward strandSMG8: 59,209,400–59,215,249, forward strandSMG8GDPD1: 59,220,467–59,275,970, forward strandGDPD1YPEL2: 59,331,591–59,401,729, forward strandYPEL2Diagram of TRIM37: 24 exons on the reverse strand of chromosome 17Exon 23: 1 known disease-causing siteExon 21: 2 known disease-causing sitesExon 20: 3 known disease-causing sitesExon 19: 8 known disease-causing sitesExon 18: 3 known disease-causing sitesExon 17: 1 known disease-causing siteExon 16: 1 known disease-causing siteExon 15: 4 known disease-causing sitesExon 14: 7 known disease-causing sitesExon 13: 3 known disease-causing sitesExon 12: 1 known disease-causing siteExon 11: 1 known disease-causing siteExon 10: 1 known disease-causing siteExon 9: 2 known disease-causing sitesExon 8: 3 known disease-causing sitesExon 7: 2 known disease-causing sitesExon 6: 1 known disease-causing siteExon 5: 2 known disease-causing sitesExon 4: 3 known disease-causing sitesExon 3: 1 known disease-causing siteExon 2: 2 known disease-causing sitesExon 1: 1 known disease-causing siteExon 24: 58,998,202–58,999,459, 1,258 basesExon 23: 59,001,598–59,001,714, 117 basesExon 22: 59,012,328–59,012,446, 119 basesExon 21: 59,015,610–59,015,799, 190 basesExon 20: 59,017,296–59,017,424, 129 basesExon 19: 59,028,415–59,028,723, 309 basesExon 18: 59,031,896–59,032,090, 195 basesExon 17: 59,041,813–59,041,898, 86 basesExon 16: 59,047,683–59,047,819, 137 basesExon 15: 59,049,178–59,049,393, 216 basesExon 14: 59,051,214–59,051,328, 115 basesExon 13: 59,056,875–59,057,054, 180 basesExon 12: 59,061,032–59,061,108, 77 basesExon 11: 59,062,567–59,062,648, 82 basesExon 10: 59,064,355–59,064,405, 51 basesExon 9: 59,070,823–59,070,947, 125 basesExon 8: 59,075,647–59,075,714, 68 basesExon 7: 59,079,754–59,079,877, 124 basesExon 6: 59,081,097–59,081,219, 123 basesExon 5: 59,084,002–59,084,089, 88 basesExon 4: 59,088,291–59,088,407, 117 basesExon 3: 59,091,300–59,091,340, 41 basesExon 2: 59,104,293–59,104,394, 102 basesExon 1: 59,106,441–59,106,880, 440 bases2422201816141210864215′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 4.5 kb of the gene's 108.7 kb; 2,895 of those bases code for the protein.

How a genome test reads TRIM37

68

positions in TRIM37 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 108.7 kb of TRIM37, introns included, not only the 4.5 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.). TRIM37 gene: tripartite motif containing 37. Retrieved 17 October 2026, from https://dantelabs.com/genes/trim37

Vancouver

Dante Labs. TRIM37 gene: tripartite motif containing 37 [Internet]. [cited 17 October 2026]. Available from: https://dantelabs.com/genes/trim37

One test. A lifetime of answers.

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

Get my Genome Test