Assay Details
Target Gene Details
Entrez Gene ID: | 29899 |
Gene Name: | G-protein signaling modulator 2 |
Gene Aliases: |
CMCS, DFNB82, LGN, PINS |
Location: |
Chr.1:108875350-108934335 on Build GRCh38 |
Assay Gene Location: | Within Intron 1 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
GPSM2 | XM_011541301.2 | XP_011539603.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
esv3587140 | Chr.1:108842339 - 108891089 on Build GRCh38 | Gain | AKNAD1 GPSM2 SPATA42 |
nsv1005738 | Chr.1:108868275 - 108917679 on Build GRCh38 | Loss | GPSM2 |
nsv547425 | Chr.1:108873603 - 109035828 on Build GRCh38 | Gain | CLCC1 GPSM2 WDR47 |
esv3587141 | Chr.1:108866483 - 108915393 on Build GRCh38 | Loss | GPSM2 |
More Information
Additional Information:
For this assay, SNP(s) [rs72982798] 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 |