Assay Details
Target Gene Details
Entrez Gene ID: | 5995 |
Gene Name: | retinal G protein coupled receptor |
Gene Aliases: |
RP44 |
Location: |
Chr.10:84245053-84259188 on Build GRCh38 |
Assay Gene Location: | Within Intron 5 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
RGR | NM_001012720.1 | NP_001012738.1 | ||
NM_001012722.1 | NP_001012740.1 | |||
NM_002921.3 | NP_002912.2 | |||
BC011349.1 | AAH11349.1 | |||
BG912392.1 | ||||
BX641033.1 | ||||
KU178307.1 | ||||
KU178308.1 | ||||
U14910.1 | AAA56748.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv527522 | Chr.10:84252173 - 84272997 on Build GRCh38 | Loss | RGR |
nsv1046749 | Chr.10:83270389 - 84629720 on Build GRCh38 | Gain | C10orf99 GHITM RGR LRIT1 LOC105378397 CDHR1 HOST2 LINC00858 LRIT2 CCSER2 |
nsv551745 | Chr.10:83260366 - 84632635 on Build GRCh38 | Gain | C10orf99 GHITM RGR LRIT1 LOC105378397 CDHR1 HOST2 LINC00858 LRIT2 CCSER2 |
More Information
Additional Information:
For this assay, SNP(s) [rs74145780] 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 Intronic Non-exonic DGV Variation |