Genomic Map
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Target Gene Details
Entrez Gene ID: | 136 |
Gene Name: | adenosine A2b receptor |
Gene Aliases: |
ADORA2 |
Location: |
Chr.17:15927781-15975896 on Build GRCh38 |
Assay Gene Location: | Within Exon 3 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| ADORA2B | NM_000676.2 | NP_000667.1 | ||
| XM_011523659.2 | XP_011521961.1 | |||
| XM_011523661.2 | 1 | 153 | XP_011521963.1 | |
| X68487.1 | CAA48505.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv1061987 | Chr.17:15906703 - 15951821 on Build GRCh38 | Loss |
 ADORA2B
|
| esv2715702 | Chr.17:15750514 - 16668268 on Build GRCh38 | Deletion |
ADORA2B
MEIS3P1
TRPV2
SNORD65
LRRC75A-AS1
PIGL
CCDC144A
NCOR1
ZNF624
CDRT15P2
CENPV
SNORD49B
TTC19
ZSWIM7
LRRC75A
MIR1288
UBB
SNORD49A
LOC101928567
ZNF287
|
| dgv3107n100 | Chr.17:15703953 - 16150198 on Build GRCh38 | Gain |
ADORA2B
ZSWIM7
MEIS3P1
ZNF286A
NCOR1
LOC101928567
CDRT15P2
TBC1D26
TTC19
|
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Additional Information:
For this assay, SNP(s) [rs79347649] 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
Exonic
DGV Variation
|
Panther Classification:
Gene Ontology Categories:
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