Assay Details
Target Gene Details
Entrez Gene ID: | 128434 |
Gene Name: | V-set and transmembrane domain containing 2 like |
Gene Aliases: |
C20orf102, dJ1118M15.2 |
Location: |
Chr.20:37903097-37945350 on Build GRCh38 |
Assay Gene Location: | Within Intron 1 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
VSTM2L | NM_080607.2 | NP_542174.1 | ||
XM_011528530.1 | XP_011526832.1 | |||
AK056177.1 | BAB71113.1 | |||
AL834410.1 | CAD39072.2 | |||
BC033818.1 | AAH33818.1 | |||
BE905791.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv833970 | Chr.20:37817358 - 37909509 on Build GRCh38 | Gain |
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nsv1066778 | Chr.20:37849676 - 37921323 on Build GRCh38 | Gain |
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nsv1057334 | Chr.20:37793679 - 38139909 on Build GRCh38 | Loss |
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More Information
Additional Information:
For this assay, SNP(s) [rs77609510] 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: |
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Panther Classification:
Gene Ontology Categories:
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