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MIRAGE
P2X purinoceptor 2
Summary
- UniProt ID
- Q9UBL9
- Gene Symbol
- P2RX2 P2X2
- Gene ID
- 22953
- Organism
- Homo sapiens (human)
Annotation
- Keyword
- ATP-binding Alternative splicing Cell membrane Disease variant Disulfide bond Glycoprotein Hearing Ligand-gated ion channel Non-syndromic deafness Proteomics identification Receptor Reference proteome Transmembrane helix
Gene Ontology (GO)
| GO Term | Evidence Code | Reference |
|---|---|---|
| response to hypoxia |
|
|
| response to ischemia | ||
| detection of hypoxic conditions in blood by carotid body chemoreceptor signaling |
|
|
| neuromuscular synaptic transmission |
|
|
| neuromuscular junction development |
|
|
GO Hierarchy
biological process
biological regulation [inference]
regulation of biological process [inference]
regulation of localization [inference]
positive regulation of biological process [inference]
regulation of cellular process [inference]
| GO Term | Evidence Code | Reference |
|---|---|---|
| plasma membrane | ||
| plasma membrane | ||
| plasma membrane | ||
| plasma membrane | ||
| plasma membrane |
GO Hierarchy
| GO Term | Evidence Code | Reference |
|---|---|---|
| purinergic nucleotide receptor activity | ||
| purinergic nucleotide receptor activity | ||
| extracellularly ATP-gated monoatomic cation channel activity | ||
| extracellularly ATP-gated monoatomic cation channel activity | ||
| extracellularly ATP-gated monoatomic cation channel activity |
GO Hierarchy
Sequence
MAAAQPKYPAGATARRLARGCWSALWDYETPKVIVVRNRRLGVLYRAVQLLILLYFVWYVFIVQKSYQESETGPESSIITKVKGITTSEHKVWDVEEYVKPPEGGSVFSIITRVEATHSQTQGTCPESIRVHNATCLSDADCVAGELDMLGNGLRTGRCVPYYQGPSKTCEVFGWCPVEDGASVSQFLGTMAPNFTILIKNSIHYPKFHFSKGNIADRTDGYLKRCTFHEASDLYCPIFKLGFIVEKAGESFTELAHKGGVIGVIINWDCDLDLPASECNPKYSFRRLDPKHVPASSGYNFRFAKYYKINGTTTRTLIKAYGIRIDVIVHGQAGKFSLIPTIINLATALTSVGVGSFLCDWILLTFMNKNKVYSHKKFDKVCTPSHPSGSWPVTLARVLGQAPPEPGHRSEDQHPSPPSGQEGQQGAECGPAFPPLRPCPISAPSEQMVDTPASEPAQASTPTDPKGLAQL
Glycosylation Sites
Feature
: Glycosylation Site from GlyGen
: Glycosylation Site from UniProt
Pathway
| Pathway Name | Organism |
|---|---|
| Elevation of cytosolic Ca2+ levels | Homo sapiens |
| Platelet homeostasis | Homo sapiens |
Disease
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0110567 | autosomal dominant nonsyndromic deafness 41 |
