Assay Details
Target Gene Details
Entrez Gene ID: | 83930 |
Gene Name: | STARD3 N-terminal like |
Gene Aliases: |
MENTHO |
Location: |
Chr.7:38178206-38230671 on Build GRCh38 |
Assay Gene Location: | Within Intron 2 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
STARD3NL | NM_032016.3 | NP_114405.1 | ||
XM_005249880.1 | XP_005249937.1 | |||
XM_005249881.2 | XP_005249938.1 | |||
XM_017012694.1 | XP_016868183.1 | |||
XM_017012695.1 | XP_016868184.1 | |||
AJ492267.1 | CAD37353.1 | |||
AK091579.1 | ||||
AK315404.1 | ||||
AY358645.1 | AAQ89008.1 | |||
BC005959.1 | AAH05959.1 | |||
DT218211.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
dgv89n68 | Chr.7:38133386 - 38350917 on Build GRCh38 | Gain | STARD3NL TARP TRGV5 TRGV9 TRGC2 TRGV7 TRG-AS1 |
esv2759524 | Chr.7:38179101 - 38483855 on Build GRCh38 | Loss | STARD3NL TARP TRGV5 TRGV9 TRGC2 AMPH TRGV7 TRG-AS1 TRGV3 |
esv2762664 | Chr.7:38162212 - 38188878 on Build GRCh38 | Loss | STARD3NL |
More Information
Additional Information:
For this assay, SNP(s) [rs77039344] 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 |