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Gene

GON4L

gon-4 like

Summary

Cytogenetic location
1q22
Coordinates
Chromosome 1: 155,749,659–155,857,214 (GRCh38)
Exons
32 exons across 107.6 kb
Protein
2,241 amino acids
Also known as
FLJ20203, GON-4, YARP
Previous symbols
GON4
MANE Select transcript
ENST00000368331.6NM_001282860.2
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 GON4L yet. The test sequences your whole genome, so your data includes it all the same.

How GON4L is laid out

  • Coding sequence
  • Untranslated region
  • Intron
  • Direction of transcription
  • Known disease-causing sites
  • Stretches short reads find hard
Chromosome 1, with a bracket where GON4L sits. GON4L and 28 genes near it on chromosome 1, from 155,303,437 to 156,303,436.Chromosome 11q22p36.33p36.32p36.31p36.23p36.22p36.21p36.13p36.12p36.11p35.3p35.2p35.1p34.3p34.2p34.1p33p32.3p32.2p32.1p31.3p31.2p31.1p22.3p22.2p22.1p21.3p21.2p21.1p13.3p13.2p13.1p12p11.2p11.1q11q12q21.1q21.2q21.3q22q23.1q23.2q23.3q24.1q24.2q24.3q25.1q25.2q25.3q31.1q31.2q31.3q32.1q32.2q32.3q41q42.11q42.12q42.13q42.2q42.3q43q44155.4 Mb155.6 Mb155.8 Mb156 Mb156.2 MbFDPS: 155,304,786–155,320,666, forward strandFDPSRUSC1: 155,320,739–155,331,422, forward strandRUSC1ASH1L: 155,335,268–155,563,162, reverse strandASH1LMSTO1: 155,563,235–155,616,644, forward strandMSTO1: 155,626,755–155,648,640, reverse strandYY1AP1: 155,659,446–155,689,334, reverse strandYY1AP1DAP3: 155,687,833–155,740,132, forward strandDAP3GON4L: 155,749,659–155,857,214, reverse strandGON4LSYT11: 155,859,449–155,885,199, forward strandSYT11RIT1: 155,897,808–155,911,408, reverse strandRIT1KHDC4: 155,913,043–155,934,416, reverse strandKHDC4RXFP4: 155,941,638–155,943,087, forward strandRXFP4ARHGEF2: 155,944,685–156,007,070, reverse strandARHGEF2SSR2: 156,009,041–156,020,972, reverse strandSSR2UBQLN4: 156,026,961–156,053,814, reverse strandUBQLN4LAMTOR2: 156,053,916–156,058,817, forward strandLAMTOR2RAB25: 156,061,147–156,070,514, forward strandRAB25MEX3A: 156,072,013–156,082,465, reverse strandMEX3ALMNA: 156,082,572–156,140,085, forward strandLMNASEMA4A: 156,147,366–156,178,869, forward strandSEMA4ASLC25A44: 156,193,932–156,212,796, forward strandSLC25A44PMF1-BGLAP: 156,212,982–156,243,332, forward strandPMF1-BGLAPPMF1: 156,212,989–156,240,585, forward strandPMF1BGLAP: 156,242,154–156,243,317, forward strandBGLAPPAQR6: 156,243,318–156,248,647, reverse strandSMG5: 156,249,223–156,282,862, reverse strandTMEM79: 156,282,928–156,293,185, forward strandTMEM79GLMP: 156,290,088–156,295,699, reverse strandGLMPVHLL: 156,298,624–156,299,307, reverse strandVHLLDiagram of GON4L: 32 exons on the reverse strand of chromosome 1Exon 2: 1 known disease-causing siteExon 32: 155,749,659–155,750,733, 1,075 basesExon 31: 155,751,767–155,751,869, 103 basesExon 30: 155,751,960–155,752,590, 631 basesExon 29: 155,753,204–155,753,414, 211 basesExon 28: 155,754,375–155,754,488, 114 basesExon 27: 155,756,958–155,757,077, 120 basesExon 26: 155,757,180–155,757,323, 144 basesExon 25: 155,757,891–155,758,034, 144 basesExon 24: 155,760,444–155,760,641, 198 basesExon 23: 155,762,190–155,762,374, 185 basesExon 22: 155,763,312–155,763,564, 253 basesExon 21: 155,765,000–155,766,709, 1,710 basesExon 20: 155,767,425–155,767,541, 117 basesExon 19: 155,771,067–155,771,217, 151 basesExon 18: 155,773,066–155,773,210, 145 basesExon 17: 155,775,002–155,775,173, 172 basesExon 16: 155,776,395–155,776,481, 87 basesExon 15: 155,777,622–155,777,820, 199 basesExon 14: 155,783,986–155,784,089, 104 basesExon 13: 155,785,334–155,785,374, 41 basesExon 12: 155,795,050–155,795,151, 102 basesExon 11: 155,804,949–155,805,141, 193 basesExon 10: 155,813,634–155,813,804, 171 basesExon 9: 155,814,330–155,814,449, 120 basesExon 8: 155,815,805–155,815,900, 96 basesExon 7: 155,816,212–155,816,262, 51 basesExon 6: 155,820,606–155,820,656, 51 basesExon 5: 155,821,474–155,821,548, 75 basesExon 4: 155,822,286–155,822,476, 191 basesExon 3: 155,826,837–155,827,028, 192 basesExon 2: 155,853,276–155,853,806, 531 basesExon 1: 155,857,147–155,857,214, 68 bases322015′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 7.7 kb of the gene's 107.6 kb; 6,726 of those bases code for the protein.

How a genome test reads GON4L

1

position in GON4L 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 107.6 kb of GON4L, introns included, not only the 7.7 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.). GON4L gene: gon-4 like. Retrieved 17 October 2026, from https://dantelabs.com/genes/gon4l

Vancouver

Dante Labs. GON4L gene: gon-4 like [Internet]. [cited 17 October 2026]. Available from: https://dantelabs.com/genes/gon4l

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