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Gene

RGR

retinal G protein coupled receptor

Summary

Cytogenetic location
10q23.1
Coordinates
Chromosome 10: 84,245,053–84,259,960 (GRCh38)
Exons
7 exons across 14.9 kb
Protein
291 amino acids
Also known as
RP44
MANE Select transcript
ENST00000652092.2NM_001012720.2
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 RGR yet. The test sequences your whole genome, so your data includes it all the same.

How RGR is laid out

  • Coding sequence
  • Untranslated region
  • Intron
  • Direction of transcription
  • Known disease-causing sites
  • Stretches short reads find hard
Chromosome 10, with a bracket where RGR sits. RGR and 6 genes near it on chromosome 10, from 83,752,507 to 84,752,506.Chromosome 1010q23.1p15.3p15.2p15.1p14p13p12.33p12.32p12.31p12.2p12.1p11.23p11.22p11.21p11.1q11.1q11.21q11.22q11.23q21.1q21.2q21.3q22.1q22.2q22.3q23.1q23.2q23.31q23.32q23.33q24.1q24.2q24.31q24.32q24.33q25.1q25.2q25.3q26.11q26.12q26.13q26.2q26.383.8 Mb84 Mb84.2 Mb84.4 Mb84.6 MbGHITM: 84,139,482–84,154,841, forward strandGHITMGPR15LG: 84,173,759–84,185,294, forward strandGPR15LGCDHR1: 84,194,514–84,221,689, forward strandCDHR1LRIT2: 84,220,571–84,225,544, reverse strandLRIT2LRIT1: 84,228,873–84,241,546, reverse strandLRIT1RGR: 84,245,053–84,259,960, forward strandRGRCCSER2: 84,328,542–84,518,521, forward strandCCSER2Diagram of RGR: 7 exons on the forward strand of chromosome 10Exon 2: 1 known disease-causing siteExon 7: 2 known disease-causing sitesExon 1: 84,245,053–84,245,169, 117 basesExon 2: 84,247,591–84,247,747, 157 basesExon 3: 84,248,922–84,249,043, 122 basesExon 4: 84,252,857–84,253,010, 154 basesExon 5: 84,254,326–84,254,443, 118 basesExon 6: 84,257,893–84,258,006, 114 basesExon 7: 84,258,508–84,259,960, 1,453 bases12345675′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 2.2 kb of the gene's 14.9 kb; 876 of those bases code for the protein.

How a genome test reads RGR

3

positions in RGR 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 14.9 kb of RGR, introns included, not only the 2.2 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.). RGR gene: retinal G protein coupled receptor. Retrieved 17 October 2026, from https://dantelabs.com/genes/rgr

Vancouver

Dante Labs. RGR gene: retinal G protein coupled receptor [Internet]. [cited 17 October 2026]. Available from: https://dantelabs.com/genes/rgr

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