Assay Details
Target Gene Details
Entrez Gene ID: | 55799 |
Gene Name: | calcium voltage-gated channel auxiliary subunit alpha2delta 3 |
Gene Aliases: |
HSA272268 |
Location: |
Chr.3:54122594-55074557 on Build GRCh38 |
Assay Gene Location: | Within Intron 11 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
CACNA2D3 | NM_018398.2 | NP_060868.2 | ||
XM_005265318.2 | XP_005265375.1 | |||
XM_011533946.2 | XP_011532248.1 | |||
XM_011533947.2 | XP_011532249.1 | |||
XM_011533948.2 | XP_011532250.1 | |||
XM_011533949.2 | XP_011532251.1 | |||
XM_011533950.2 | XP_011532252.1 | |||
XM_011533951.2 | XP_011532253.1 | |||
XM_011533952.2 | XP_011532254.1 | |||
XM_011533953.2 | XP_011532255.1 | |||
XM_017006850.1 | XP_016862339.1 | |||
XM_017006851.1 | XP_016862340.1 | |||
XM_017006852.1 | XP_016862341.1 | |||
AF516696.1 | AAN06673.1 | |||
AJ272213.1 | CAB75878.1 | |||
AJ272268.1 | CAB75962.1 | |||
AK299718.1 | ||||
AK307449.1 | ||||
BC137502.1 | ||||
BC137505.1 |
Target Gene Details
Entrez Gene ID: | 790952 |
Gene Name: | embryonic stem cell related (non-protein coding) |
Gene Aliases: |
HESRG |
Location: |
Chr.3:54632124-54639857 on Build GRCh38 |
Assay Gene Location: | Within Intron 2 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
ESRG | NR_027122.1 | |||
DQ445779.2 | ABD92927.1 | |||
KM363598.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv834700 | Chr.3:54603347 - 54769869 on Build GRCh38 | Gain |
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nsv517851 | Chr.3:54375499 - 55705332 on Build GRCh38 | Gain |
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nsv1014595 | Chr.3:53910446 - 54812727 on Build GRCh38 | Loss |
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nsv525644 | Chr.3:54619289 - 54675960 on Build GRCh38 | Gain |
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![](/order/genome-database/details/genotyping/assets/img/arrow_icon_up_black.png)
More Information
Additional Information:
For this assay, SNP(s) [rs77353063] 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:
![](/order/genome-database/details/genotyping/assets/img/arrow_icon_up_black.png)