RGS5 regulator of G protein signaling 5
Gene ID: 8490, updated on 10-Oct-2024Gene type: protein coding
Also known as: MST092; MST106; MST129; MSTP032; MSTP092; MSTP106; MSTP129
- See all available tests in GTR for this gene
- Go to complete Gene record for RGS5
- Go to Variation Viewer for RGS5 variants
Summary
This locus represents naturally occurring readthrough transcription between the neighboring LOC127814295 (uncharacterized LOC127814295) and RGS5 (regulator of G-protein signaling 5) genes on chromosome 1. Some variants of the readthrough transcript encode novel proteins with unique N-termini. [provided by RefSeq, Nov 2022]
Associated conditions
See all available tests in GTR for this gene
| Description | Tests |
|---|---|
| Essential hypertension, genetic | See labs |
| Genome-wide association study for biomarker identification of Rapamycin and Everolimus using a lymphoblastoid cell line system. GeneReviews: Not available | |
| Genome-wide association study of liver enzymes in korean children. GeneReviews: Not available |
Genomic context
- Location:
- 1q23.3
- Sequence:
- Chromosome: 1; NC_000001.11 (163142299..163321735, complement)
- Total number of exons:
- 10
Variation
| Resource | Links for this gene |
|---|---|
| ClinVar | Variants reported to ClinVar |
| dbVar | Studies and variants |
| SNP | Variation Viewer for RGS5 variants |
| Genome viewer | Explore NCBI-annotated and select non-NCBI annotated genome assemblies |
- ClinVarRelated medical variations
- dbVarLink from Gene to dbVar
- MedGenRelated information in MedGen
- OMIMLink to related OMIM entry
- PubMed (OMIM)Gene links to PubMed derived from omim_pubmed_cited links
- RefSeq RNAsLink to Nucleotide RefSeq RNAs
- RefSeqGeneLink to Nucleotide RefSeqGenes
- RGS5 database
- Variation ViewerRelated Variants
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