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Gene

GOLGA2

golgin A2

Summary

Cytogenetic location
9q34.11
Coordinates
Chromosome 9: 128,255,829–128,276,007 (GRCh38)
Exons
27 exons across 20.2 kb
Protein
1,029 amino acids
Also known as
GM130, golgin-95
MANE Select transcript
ENST00000611957.5NM_001366244.2
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 GOLGA2 yet. The test sequences your whole genome, so your data includes it all the same.

How GOLGA2 is laid out

  • Coding sequence
  • Untranslated region
  • Intron
  • Direction of transcription
  • Known disease-causing sites
  • Stretches short reads find hard
Chromosome 9, with a bracket where GOLGA2 sits. GOLGA2 and 32 genes near it on chromosome 9, from 127,765,918 to 128,765,917.Chromosome 99q34.11p24.3p24.2p24.1p23p22.3p22.2p22.1p21.3p21.2p21.1p13.3p13.2p13.1p12p11.2p11.1q11q12q13q21.11q21.12q21.13q21.2q21.31q21.32q21.33q22.1q22.2q22.31q22.32q22.33q31.1q31.2q31.3q32q33.1q33.2q33.3q34.11q34.12q34.13q34.2q34.3127.8 Mb128 Mb128.2 Mb128.4 Mb128.6 MbSH2D3C: 127,738,317–127,778,771, reverse strandSH2D3CCDK9: 127,785,252–127,792,871, forward strandCDK9FPGS: 127,794,597–127,815,065, forward strandFPGSENG: 127,811,130–127,855,232, reverse strandENGAK1: 127,866,435–127,878,558, reverse strandAK1: 127,867,850–127,906,022, reverse strandST6GALNAC6: 127,885,320–127,906,632, reverse strandST6GALNAC4: 127,906,919–127,917,057, reverse strandST6GALNAC4PIP5KL1: 127,920,881–127,930,823, reverse strandPIP5KL1DPM2: 127,935,090–127,937,879, reverse strandDPM2EEIG1: 127,939,491–127,981,075, reverse strandEEIG1NAIF1: 128,061,233–128,068,206, reverse strandNAIF1SLC25A25: 128,068,169–128,109,245, forward strandSLC25A25PTGES2: 128,120,693–128,128,462, reverse strandPTGES2LCN2: 128,149,071–128,153,454, forward strandLCN2BBLN: 128,160,219–128,163,928, forward strandBBLNCIZ1: 128,161,233–128,204,482, reverse strandCIZ1DNM1: 128,191,655–128,255,254, forward strandDNM1GOLGA2: 128,255,829–128,276,007, reverse strandGOLGA2SWI5: 128,275,379–128,316,123, forward strandSWI5TRUB2: 128,305,159–128,322,741, reverse strandTRUB2COQ4: 128,322,483–128,334,073, forward strandCOQ4SLC27A4: 128,340,475–128,363,283, forward strandSLC27A4URM1: 128,371,341–128,392,017, forward strandURM1CERCAM: 128,411,575–128,437,362, forward strandCERCAMODF2: 128,455,181–128,502,162, forward strandODF2GLE1: 128,504,655–128,543,874, forward strandGLE1SPTAN1: 128,552,558–128,633,663, forward strandSPTAN1DYNC2I2: 128,633,646–128,656,847, reverse strandDYNC2I2SET: 128,683,424–128,696,400, forward strandSETPKN3: 128,702,489–128,720,924, forward strandPKN3ZDHHC12: 128,720,862–128,724,146, reverse strandZDHHC12ZER1: 128,729,785–128,772,414, reverse strandZER1Diagram of GOLGA2: 27 exons on the reverse strand of chromosome 9Exon 20: 1 known disease-causing siteExon 18: 1 known disease-causing siteExon 14: 1 known disease-causing siteExon 8: 1 known disease-causing siteExon 27: 128,255,829–128,257,281, 1,453 basesExon 26: 128,257,369–128,257,525, 157 basesExon 25: 128,257,601–128,257,707, 107 basesExon 24: 128,257,790–128,257,892, 103 basesExon 23: 128,257,980–128,258,198, 219 basesExon 22: 128,258,455–128,258,570, 116 basesExon 21: 128,259,007–128,259,082, 76 basesExon 20: 128,259,167–128,259,391, 225 basesExon 19: 128,260,076–128,260,189, 114 basesExon 18: 128,260,465–128,260,802, 338 basesExon 17: 128,261,172–128,261,259, 88 basesExon 16: 128,261,454–128,261,561, 108 basesExon 15: 128,261,668–128,261,757, 90 basesExon 14: 128,262,563–128,262,704, 142 basesExon 13: 128,263,034–128,263,092, 59 basesExon 12: 128,265,585–128,265,691, 107 basesExon 11: 128,265,788–128,265,881, 94 basesExon 10: 128,265,970–128,266,020, 51 basesExon 9: 128,266,287–128,266,325, 39 basesExon 8: 128,267,194–128,267,274, 81 basesExon 7: 128,267,458–128,267,517, 60 basesExon 6: 128,267,934–128,267,997, 64 basesExon 5: 128,268,117–128,268,160, 44 basesExon 4: 128,268,420–128,268,524, 105 basesExon 3: 128,272,785–128,272,865, 81 basesExon 2: 128,273,850–128,273,972, 123 basesExon 1: 128,275,893–128,276,007, 115 bases2725201510515′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 4.4 kb of the gene's 20.2 kb; 3,090 of those bases code for the protein.

How a genome test reads GOLGA2

4

positions in GOLGA2 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 20.2 kb of GOLGA2, introns included, not only the 4.4 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.). GOLGA2 gene: golgin A2. Retrieved 17 October 2026, from https://dantelabs.com/genes/golga2

Vancouver

Dante Labs. GOLGA2 gene: golgin A2 [Internet]. [cited 17 October 2026]. Available from: https://dantelabs.com/genes/golga2

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