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Gene

RGS9

regulator of G protein signaling 9

Summary

Cytogenetic location
17q24.1
Coordinates
Chromosome 17: 65,137,370–65,227,703 (GRCh38)
Exons
19 exons across 90.3 kb
Protein
674 amino acids
Also known as
PERRS, RGS9L, MGC26458, MGC111763
MANE Select transcript
ENST00000262406.10NM_003835.4
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 RGS9 yet. The test sequences your whole genome, so your data includes it all the same.

How RGS9 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 RGS9 sits. RGS9 and 5 genes near it on chromosome 17, from 64,682,537 to 65,682,536.Chromosome 1717q24.1p13.3p13.2p13.1p12p11.2p11.1q11.1q11.2q12q21.1q21.2q21.31q21.32q21.33q22q23.1q23.2q23.3q24.1q24.2q24.3q25.1q25.2q25.364.8 Mb65 Mb65.2 Mb65.4 Mb65.6 MbLRRC37A3: 64,854,130–64,919,488, reverse strandLRRC37A3GNA13: 65,009,289–65,056,839, reverse strandGNA13RGS9: 65,137,370–65,227,703, forward strandRGS9AXIN2: 65,528,561–65,562,067, reverse strandAXIN2: 65,538,102–65,641,033, reverse strandCEP112: 65,635,537–66,192,251, reverse strandCEP112Diagram of RGS9: 19 exons on the forward strand of chromosome 17Exon 2: 1 known disease-causing siteExon 13: 1 known disease-causing siteExon 17: 1 known disease-causing siteExon 1: 65,137,370–65,137,597, 228 basesExon 2: 65,153,422–65,153,518, 97 basesExon 3: 65,158,295–65,158,345, 51 basesExon 4: 65,160,233–65,160,339, 107 basesExon 5: 65,160,536–65,160,587, 52 basesExon 6: 65,160,851–65,160,909, 59 basesExon 7: 65,163,013–65,163,089, 77 basesExon 8: 65,168,200–65,168,281, 82 basesExon 9: 65,177,732–65,177,803, 72 basesExon 10: 65,189,286–65,189,315, 30 basesExon 11: 65,190,175–65,190,236, 62 basesExon 12: 65,193,543–65,193,656, 114 basesExon 13: 65,197,126–65,197,241, 116 basesExon 14: 65,201,993–65,202,080, 88 basesExon 15: 65,204,163–65,204,301, 139 basesExon 16: 65,207,922–65,208,007, 86 basesExon 17: 65,210,488–65,210,605, 118 basesExon 18: 65,225,002–65,225,486, 485 basesExon 19: 65,227,275–65,227,703, 429 bases151015195′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 2.5 kb of the gene's 90.3 kb; 2,025 of those bases code for the protein.

How a genome test reads RGS9

3

positions in RGS9 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 90.3 kb of RGS9, introns included, not only the 2.5 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.). RGS9 gene: regulator of G protein signaling 9. Retrieved 16 October 2026, from https://dantelabs.com/genes/rgs9

Vancouver

Dante Labs. RGS9 gene: regulator of G protein signaling 9 [Internet]. [cited 16 October 2026]. Available from: https://dantelabs.com/genes/rgs9

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