Assay Details
Target Gene Details
Entrez Gene ID: | 80380 |
Gene Name: | programmed cell death 1 ligand 2 |
Gene Aliases: |
B7DC, Btdc, CD273, PD-L2, PDCD1L2, PDL2, bA574F11.2 |
Location: |
Chr.9:5510438-5571282 on Build GRCh38 |
Assay Gene Location: | Within Exon 1 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
PDCD1LG2 | NM_025239.3 | 1 | 194 | NP_079515.2 |
XM_005251600.3 | 1 | 301 | XP_005251657.1 | |
AF329193.1 | 1 | 178 | AAK31105.1 | |
AF344424.1 | 1 | 194 | AAK15370.1 | |
BC074766.2 | AAH74766.1 | |||
BC113678.1 | ||||
BC113680.1 | ||||
EF444806.1 | 1 | 41 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv509292 | Chr.9:5469291 - 5546768 on Build GRCh38 | Insertion |
![]() ![]() |
nsv613196 | Chr.9:5345673 - 5514372 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) [rs80027732] 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)