Genomic Map
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Target Gene Details
Entrez Gene ID: | 22953 |
Gene Name: | purinergic receptor P2X 2 |
Gene Aliases: |
DFNA41, P2X2 |
Location: |
Chr.12:132618780-132623678 on Build GRCh38 |
Assay Gene Location: | Within Exon 9 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| P2RX2 | NM_001282164.1 | NP_001269093.1 | ||
| NM_001282165.1 | 10 | 1484 | NP_001269094.1 | |
| NM_012226.4 | 9 | 1171 | NP_036358.2 | |
| NM_016318.3 | 10 | 1315 | NP_057402.1 | |
| NM_170682.3 | 11 | 1387 | NP_733782.1 | |
| NM_170683.3 | 10 | 1465 | NP_733783.1 | |
| NM_174872.2 | 9 | 1111 | NP_777361.1 | |
| NM_174873.2 | NP_777362.1 | |||
| XM_005266154.3 | 10 | 1494 | XP_005266211.1 | |
| XM_005266155.4 | XP_005266212.1 | |||
| XM_005266156.4 | XP_005266213.1 | |||
| XM_011534786.2 | 9 | 1377 | XP_011533088.1 | |
| XM_017019035.1 | XP_016874524.1 | |||
| AF109387.1 | 11 | 1314 | AAD42947.1 | |
| AF109388.1 | AAD42948.1 | |||
| AF190822.1 | 11 | 1350 | AAF19170.1 | |
| AF190823.1 | AAF19171.1 | |||
| AF190824.1 | AAF19172.1 | |||
| AF190825.1 | AAF19173.1 | |||
| AF260426.1 | 11 | 1387 | AAF74201.1 | |
| AF260427.1 | AAF74202.1 | |||
| AF260428.1 | AAF74203.1 | |||
| AF260429.1 | AAF74204.1 | |||
| AY346374.1 | AAQ54329.1 | |||
| BC109200.2 | 10 | 1447 | AAI09201.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv952512 | Chr.12:132192256 - 132711214 on Build GRCh38 | Deletion |
 LOC100996573
PGAM5
LOC105370092
PXMP2
POLE
LRCOL1
GALNT9
FBRSL1
P2RX2
MUC8
LOC100130238
LOC101928416
MIR6763
|
| nsv561109 | Chr.12:132618549 - 132626173 on Build GRCh38 | Loss |
P2RX2
POLE
|
| esv2422284 | Chr.12:132604248 - 132708921 on Build GRCh38 | Deletion |
P2RX2
PXMP2
POLE
LRCOL1
|
| nsv826563 | Chr.12:132125383 - 132622340 on Build GRCh38 | Gain |
EP400NL
LOC100996573
LOC105370092
DDX51
LRCOL1
GALNT9
FBRSL1
P2RX2
MUC8
NOC4L
LOC100130238
LOC101928416
MIR6763
|
| nsv1037074 | Chr.12:132613063 - 132801953 on Build GRCh38 | Gain |
GOLGA3
PGAM5
P2RX2
PXMP2
POLE
ANKLE2
|
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Additional Information:
For this assay, SNP(s) [rs150092274] 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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