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- Gene Symbol
- RGS5
- Assay Reference Genome
Location
Chr.1:163146993 on build GRCh38- Cytoband
- 1q23.3
Genomic Map
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Target Gene Details
Entrez Gene ID: | 8490 |
Gene Name: | regulator of G-protein signaling 5 |
Gene Aliases: |
MST092, MST106, MST129, MSTP032, MSTP092, MSTP106, MSTP129 |
Location: |
Chr.1:163142299-163321791 on Build GRCh38 |
Assay Gene Location: | Within Exon 9 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| RGS5 | NM_001195303.2 | 3 | 1060 | NP_001182232.1 |
| NM_001254748.1 | 6 | 1118 | NP_001241677.1 | |
| NM_001254749.1 | 5 | 1245 | NP_001241678.1 | |
| NM_003617.3 | 5 | 1233 | NP_003608.1 | |
| AB008109.1 | 5 | 976 | BAA22889.1 | |
| AF030108.1 | 5 | 971 | AAB84001.1 | |
| AF159570.1 | 5 | 939 | AAD40957.1 | |
| BC030059.1 | 5 | 958 | AAH30059.1 | |
| BX537427.1 | 5 | 977 | CAD97669.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| esv3890704 | Chr.1:163103712 - 163233339 on Build GRCh38 | Loss |
 RGS5
LOC101928404
|
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Additional Information:
For this assay, SNP(s) [rs79999206] are located under a primer or probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.
Set Membership: |
Intragenic
Exonic
DGV Variation
|
Panther Classification:
Gene Ontology Categories:
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