Assay Details
Target Gene Details
Entrez Gene ID: | 55105 |
Gene Name: | G-patch domain containing 2 |
Gene Aliases: |
CT110, GPATC2, PPP1R30 |
Location: |
Chr.1:217426992-217631312 on Build GRCh38 |
Assay Gene Location: | Within Intron 11 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
GPATCH2 | NM_018040.3 | NP_060510.1 | ||
XM_011509689.2 | XP_011507991.1 | |||
XM_011509690.2 | XP_011507992.1 | |||
XM_011509691.2 | XP_011507993.1 | |||
XM_011509693.2 | XP_011507995.1 | |||
XM_017001592.1 | XP_016857081.1 | |||
AK001114.1 | BAA91509.1 | |||
AK024701.1 | ||||
AK310304.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv832559 | Chr.1:217305459 - 217482303 on Build GRCh38 | Loss | GPATCH2 |
esv2762164 | Chr.1:217216609 - 217569408 on Build GRCh38 | Gain | GPATCH2 |
nsv832570 | Chr.1:217402639 - 217576576 on Build GRCh38 | Gain | GPATCH2 |
nsv1008328 | Chr.1:217300400 - 217602339 on Build GRCh38 | Gain | GPATCH2 |
More Information
Additional Information:
For this assay, SNP(s) [rs115925313] 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 |