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 | GPR139 ACSM2A GP2 TMC7 CRYM-AS1 TMEM159 KNOP1 LYRM1 NPIPB3 SYT17 DNAH3 IQCK CCP110 CLEC19A TMC5 COQ7 ZP2 UMOD PDILT ACSM2B LOC102723385 C16orf62 ACSM5 SMG1P3 DCUN1D3 ACSM3 SNX29P1 THUMPD1 GPRC5B ITPRIPL2 ERI2 LOC81691 GDE1 LOC100190986 CRYM ACSM1 ANKS4B |
More Information
Additional Information:
For this assay, SNP(s) [rs72772726] 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 |