Assay Details
Target Gene Details
Entrez Gene ID: | 124274 |
Gene Name: | G protein-coupled receptor 139 |
Gene Aliases: |
GPRg1, PGR3 |
Location: |
Chr.16:20031485-20073778 on Build GRCh38 |
Assay Gene Location: | Within Intron 2 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
GPR139 | NM_001002911.3 | NP_001002911.1 | ||
NM_001318483.1 | NP_001305412.1 | |||
AB196529.1 | BAD97440.1 | |||
AK291384.1 | ||||
AY635179.1 | AAT65818.1 | |||
BC137237.1 | ||||
BC137238.1 | ||||
DN693347.1 | ||||
KR081941.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv436835 | Chr.16:18930652 - 21500976 on Build GRCh38 | Insertion | TMC5 ITPRIPL2 THUMPD1 SNX29P1 GPR139 GP2 LYRM1 ACSM5 TMC7 COQ7 CLEC19A ACSM1 DCUN1D3 ZP2 IQCK ACSM2A ANKS4B LOC102723385 SMG1P3 KNOP1 SYT17 C16orf62 CRYM-AS1 ACSM2B LOC100190986 PDILT CRYM ERI2 GDE1 TMEM159 ACSM3 UMOD NPIPB3 CCP110 DNAH3 GPRC5B LOC81691 |
More Information
Additional Information:
For this assay, SNP(s) [rs115096920] 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 |