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 | COQ7 CRYM LYRM1 GP2 PDILT LOC81691 CRYM-AS1 ACSM1 UMOD NPIPB3 C16orf62 IQCK TMC7 KNOP1 ACSM2B SYT17 TMEM159 ANKS4B LOC102723385 CCP110 SMG1P3 DNAH3 SNX29P1 LOC100190986 DCUN1D3 ACSM3 ERI2 GDE1 THUMPD1 TMC5 GPRC5B CLEC19A ITPRIPL2 GPR139 ZP2 ACSM5 ACSM2A |
More Information
Additional Information:
For this assay, SNP(s) [rs148398537] 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 |