Assay Details
Target Gene Details
Entrez Gene ID: | 283554 |
Gene Name: | G protein-coupled receptor 137C |
Gene Aliases: |
TM7SF1L2 |
Location: |
Chr.14:52553148-52637713 on Build GRCh38 |
Assay Gene Location: | Within Intron 1 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
GPR137C | NM_001099652.1 | NP_001093122.1 | ||
AK123953.1 | ||||
AL834372.1 | CAD39035.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv826955 | Chr.14:52561923 - 52565098 on Build GRCh38 | Loss | GPR137C |
esv2670271 | Chr.14:52559510 - 52564934 on Build GRCh38 | Deletion | GPR137C |
esv2748718 | Chr.14:52559523 - 52564928 on Build GRCh38 | Deletion | GPR137C |
esv3634524 | Chr.14:52559500 - 52564925 on Build GRCh38 | Loss | GPR137C |
More Information
Additional Information:
For this assay, SNP(s) [rs72684249] 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 |