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Gene

TRAF7

TNF receptor associated factor 7

Summary

Cytogenetic location
16p13.3
Coordinates
Chromosome 16: 2,155,782–2,178,129 (GRCh38)
Exons
21 exons across 22.3 kb
Protein
670 amino acids
Also known as
RNF119, DKFZp586I021, MGC7807
Previous symbols
RFWD1
MANE Select transcript
ENST00000326181.11NM_032271.3
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 TRAF7 yet. The test sequences your whole genome, so your data includes it all the same.

How TRAF7 is laid out

  • Coding sequence
  • Untranslated region
  • Intron
  • Direction of transcription
  • Known disease-causing sites
  • Stretches short reads find hard
Chromosome 16, with a bracket where TRAF7 sits. TRAF7 and 49 genes near it on chromosome 16, from 1,666,956 to 2,666,955.Chromosome 1616p13.3p13.3p13.2p13.13p13.12p13.11p12.3p12.2p12.1p11.2p11.1q11.1q11.2q12.1q12.2q13q21q22.1q22.2q22.3q23.1q23.2q23.3q24.1q24.2q24.31.8 Mb2 Mb2.2 Mb2.4 Mb2.6 MbCRAMP1: 1,612,337–1,677,908, forward strandCRAMP1: 1,632,259–1,686,715, forward strandJPT2: 1,678,256–1,702,859, forward strandJPT2MAPK8IP3: 1,706,166–1,770,374, forward strandNME3: 1,770,317–1,771,746, reverse strandMRPS34: 1,771,889–1,773,487, reverse strandEME2: 1,772,283–1,781,708, forward strandSPSB3: 1,776,710–1,793,700, reverse strandNUBP2: 1,782,932–1,789,189, forward strandNUBP2IGFALS: 1,790,227–1,794,971, reverse strandIGFALSHAGH: 1,795,620–1,827,187, reverse strandHAGHFAHD1: 1,826,967–1,842,053, forward strandFAHD1MEIOB: 1,833,986–1,884,294, reverse strandMEIOBHS3ST6: 1,911,475–1,918,415, reverse strandHS3ST6MSRB1: 1,935,685–1,943,270, reverse strandMSRB1RPL3L: 1,943,791–1,957,606, reverse strandNDUFB10: 1,959,500–1,962,105, forward strandRPS2: 1,961,987–1,965,510, reverse strandRNF151: 1,966,823–1,968,975, forward strandTBL3: 1,971,972–1,983,056, forward strandTBL3NOXO1: 1,978,912–1,984,636, reverse strandGFER: 1,983,699–1,987,749, forward strandGFERSYNGR3: 1,989,637–1,994,275, forward strandZNF598: 1,997,654–2,009,821, reverse strandZNF598NPW: 2,009,926–2,020,755, forward strandNPWNHERF2: 2,025,356–2,039,026, forward strandNHERF2NTHL1: 2,039,814–2,047,866, reverse strandNTHL1TSC2: 2,047,345–2,089,491, forward strandTSC2PKD1: 2,088,708–2,135,898, reverse strandPKD1RAB26: 2,140,803–2,154,165, forward strandRAB26TRAF7: 2,155,782–2,178,129, forward strandTRAF7CASKIN1: 2,177,180–2,196,788, reverse strandCASKIN1MLST8: 2,204,248–2,209,453, forward strandMLST8BRICD5: 2,209,252–2,210,905, reverse strandBRICD5PGP: 2,211,593–2,214,846, reverse strandPGPE4F1: 2,223,440–2,235,743, forward strandDNASE1L2: 2,235,816–2,238,711, forward strandECI1: 2,239,376–2,252,300, reverse strandRNPS1: 2,253,116–2,268,413, reverse strandRNPS1ABCA3: 2,275,878–2,340,788, reverse strandABCA3CCNF: 2,429,394–2,458,913, forward strandCCNFTEDC2: 2,460,085–2,464,963, forward strandTEDC2NTN3: 2,471,286–2,474,145, forward strandNTN3TBC1D24: 2,475,051–2,509,671, forward strandTBC1D24: 2,496,032–2,520,218, forward strandATP6V0C: 2,513,713–2,520,218, forward strand: 2,513,965–2,527,955, forward strandAMDHD2: 2,520,340–2,531,422, forward strandCEMP1: 2,530,035–2,531,417, reverse strandPDPK1: 2,537,969–2,603,190, forward strandPDPK1Diagram of TRAF7: 21 exons on the forward strand of chromosome 16Exon 13: 1 known disease-causing siteExon 14: 1 known disease-causing siteExon 17: 2 known disease-causing sitesExon 18: 1 known disease-causing siteExon 19: 2 known disease-causing sitesExon 20: 5 known disease-causing sitesExon 1: 2,155,782–2,155,858, 77 basesExon 2: 2,163,883–2,164,001, 119 basesExon 3: 2,165,879–2,165,936, 58 basesExon 4: 2,168,077–2,168,168, 92 basesExon 5: 2,170,614–2,170,730, 117 basesExon 6: 2,171,264–2,171,356, 93 basesExon 7: 2,171,572–2,171,605, 34 basesExon 8: 2,172,191–2,172,374, 184 basesExon 9: 2,172,465–2,172,599, 135 basesExon 10: 2,173,182–2,173,399, 218 basesExon 11: 2,173,481–2,173,554, 74 basesExon 12: 2,173,788–2,173,836, 49 basesExon 13: 2,173,921–2,174,048, 128 basesExon 14: 2,174,251–2,174,333, 83 basesExon 15: 2,175,111–2,175,150, 40 basesExon 16: 2,175,301–2,175,417, 117 basesExon 17: 2,175,500–2,175,622, 123 basesExon 18: 2,175,834–2,175,953, 120 basesExon 19: 2,176,049–2,176,180, 132 basesExon 20: 2,176,265–2,176,384, 120 basesExon 21: 2,176,560–2,178,129, 1,570 bases15101520215′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 3.7 kb of the gene's 22.3 kb; 2,013 of those bases code for the protein.

How a genome test reads TRAF7

12

positions in TRAF7 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 22.3 kb of TRAF7, introns included, not only the 3.7 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.). TRAF7 gene: TNF receptor associated factor 7. Retrieved 16 October 2026, from https://dantelabs.com/genes/traf7

Vancouver

Dante Labs. TRAF7 gene: TNF receptor associated factor 7 [Internet]. [cited 16 October 2026]. Available from: https://dantelabs.com/genes/traf7

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