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Gene

RGS9BP

regulator of G protein signaling 9 binding protein

Summary

Cytogenetic location
19q13.11
Coordinates
Chromosome 19: 32,675,848–32,678,300 (GRCh38)
Exons
1 exon across 2.5 kb
Protein
235 amino acids
Also known as
FLJ45744, PERRS, R9AP
MANE Select transcript
ENST00000334176.4NM_207391.3
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 RGS9BP yet. The test sequences your whole genome, so your data includes it all the same.

How RGS9BP is laid out

  • Coding sequence
  • Untranslated region
  • Intron
  • Direction of transcription
  • Known disease-causing sites
Chromosome 19, with a bracket where RGS9BP sits. RGS9BP and 12 genes near it on chromosome 19, from 32,177,074 to 33,177,073.Chromosome 1919q13.11p13.3p13.2p13.13p13.12p13.11p12p11q11q12q13.11q13.12q13.13q13.2q13.31q13.32q13.33q13.41q13.42q13.4332.2 Mb32.4 Mb32.6 Mb32.8 Mb33 MbZNF507: 32,345,594–32,387,667, forward strandZNF507DPY19L3: 32,405,543–32,485,895, forward strandDPY19L3PDCD5: 32,581,062–32,587,453, forward strandPDCD5ANKRD27: 32,597,000–32,676,597, reverse strandANKRD27RGS9BP: 32,675,848–32,678,300, forward strandRGS9BPNUDT19: 32,691,786–32,714,101, forward strandNUDT19TDRD12: 32,719,735–32,829,580, forward strandTDRD12SLC7A9: 32,830,508–32,869,805, reverse strandSLC7A9CEP89: 32,875,925–32,972,015, reverse strandCEP89FAAP24: 32,972,209–32,978,721, forward strandFAAP24RHPN2: 32,978,592–33,064,888, reverse strandRHPN2GPATCH1: 33,080,899–33,130,956, forward strandGPATCH1WDR88: 33,132,092–33,175,799, forward strandWDR88Diagram of RGS9BP: one exon on the forward strand of chromosome 19Exon 1: 3 known disease-causing sitesExon 1: 32,675,848–32,678,300, 2,453 bases15′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 2.5 kb; 708 of those bases code for the protein.

How a genome test reads RGS9BP

3

positions in RGS9BP 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 2.5 kb of RGS9BP, 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.). RGS9BP gene: regulator of G protein signaling 9 binding protein. Retrieved 17 October 2026, from https://dantelabs.com/genes/rgs9bp

Vancouver

Dante Labs. RGS9BP gene: regulator of G protein signaling 9 binding protein [Internet]. [cited 17 October 2026]. Available from: https://dantelabs.com/genes/rgs9bp

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