Assay Details
Target Gene Details
Entrez Gene ID: | 6263 |
Gene Name: | ryanodine receptor 3 |
Gene Aliases: |
RYR-3 |
Location: |
Chr.15:33310773-33866103 on Build GRCh38 |
Assay Gene Location: | Within Intron 1 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
RYR3 | NM_001036.4 | NP_001027.3 | ||
NM_001243996.2 | NP_001230925.1 | |||
XM_011521880.2 | XP_011520182.1 | |||
XM_017022468.1 | XP_016877957.1 | |||
XM_017022469.1 | XP_016877958.1 | |||
XM_017022471.1 | XP_016877960.1 | |||
XM_017022472.1 | XP_016877961.1 | |||
XM_017022473.1 | XP_016877962.1 | |||
XM_017022475.1 | XP_016877964.1 | |||
XM_017022476.1 | XP_016877965.1 | |||
XM_017022477.1 | XP_016877966.1 | |||
AB001025.1 | BAA23795.1 | |||
AJ001515.1 | CAA04798.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv832964 | Chr.15:33316570 - 33491817 on Build GRCh38 | Loss |
![]() |
nsv568919 | Chr.15:33346134 - 33444482 on Build GRCh38 | Loss |
![]() |
nsv1052620 | Chr.15:32612402 - 34538731 on Build GRCh38 | Gain |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
nsv832963 | Chr.15:33222597 - 33420241 on Build GRCh38 | Gain |
![]() ![]() ![]() |
esv33337 | Chr.15:31689863 - 34575097 on Build GRCh38 | Gain+Loss |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
dgv4456n54 | Chr.15:32604149 - 34557061 on Build GRCh38 | Gain |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![](/order/genome-database/details/genotyping/assets/img/arrow_icon_up_black.png)
More Information
Additional Information:
For this assay, SNP(s) [rs72725452] 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: |
![]() ![]() ![]() ![]() |
Panther Classification:
Gene Ontology Categories:
![](/order/genome-database/details/genotyping/assets/img/arrow_icon_up_black.png)