Assay Details
Target Gene Details
Entrez Gene ID: | 84873 |
Gene Name: | adhesion G protein-coupled receptor G7 |
Gene Aliases: |
GPR128 |
Location: |
Chr.3:100609589-100696174 on Build GRCh38 |
Assay Gene Location: | Within Intron 8 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
ADGRG7 | NM_001308362.1 | NP_001295291.1 | ||
NM_032787.2 | NP_116176.2 | |||
XM_011513245.2 | XP_011511547.1 | |||
AK027360.1 | BAB55061.1 | |||
AK131069.1 | ||||
AK172769.1 | BAD18752.1 | |||
AK295345.1 | ||||
AY181246.1 | AAO27358.1 | |||
BC113451.1 | ||||
BC130388.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
esv2751970 | Chr.3:100623466 - 100723634 on Build GRCh38 | Gain | ADGRG7 TFG |
dgv8476n54 | Chr.3:100591968 - 100736295 on Build GRCh38 | Gain | ADGRG7 TFG |
dgv8477n54 | Chr.3:100626357 - 100699750 on Build GRCh38 | Gain | ADGRG7 |
dgv182e55 | Chr.3:100580466 - 100760540 on Build GRCh38 | Gain | ADGRG7 TFG ABI3BP |
nsv1010619 | Chr.3:100634965 - 100670413 on Build GRCh38 | Gain | ADGRG7 |
dgv4831n100 | Chr.3:100621212 - 100709093 on Build GRCh38 | Gain | ADGRG7 |
esv2763708 | Chr.3:100599084 - 100723665 on Build GRCh38 | Gain | ADGRG7 TFG |
nsv516418 | Chr.3:100605598 - 100714748 on Build GRCh38 | Gain | ADGRG7 TFG |
dgv4830n100 | Chr.3:100605431 - 100729339 on Build GRCh38 | Gain | ADGRG7 TFG |
dgv183e55 | Chr.3:100623649 - 100774218 on Build GRCh38 | Gain | ADGRG7 TFG ABI3BP |
dgv614n27 | Chr.3:100631901 - 100714748 on Build GRCh38 | Gain | ADGRG7 TFG |
dgv1397e212 | Chr.3:100607666 - 100723653 on Build GRCh38 | Gain | ADGRG7 TFG |
dgv917e214 | Chr.3:100604090 - 100730204 on Build GRCh38 | Gain | ADGRG7 TFG |
More Information
Additional Information:
For this assay, SNP(s) [rs72921090,rs79611778] 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 |