Gene
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Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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5032 |
Gene nameGene Name - the full gene name approved by the HGNC.
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Purinergic receptor P2Y11 |
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
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P2RY11 |
SynonymsGene synonyms aliases
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P2Y11 |
ChromosomeChromosome number
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19 |
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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19p13.2 |
SummarySummary of gene provided in NCBI Entrez Gene.
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The product of this gene belongs to the family of G-protein coupled receptors. This family has several receptor subtypes with different pharmacological selectivity, which overlaps in some cases, for various adenosine and uridine nucleotides. This receptor |
miRNAmiRNA information provided by mirtarbase database.
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Gene ontology (GO)Gene ontology information of associated ontologies with gene provided by GO database.
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Other IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
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Protein
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UniProt ID |
Q96G91 |
Protein name |
P2Y purinoceptor 11 (P2Y11) |
Protein function |
Receptor for ATP and ADP coupled to G-proteins that activate both phosphatidylinositol-calcium and adenylyl cyclase second messenger systems. Not activated by UTP or UDP. |
Family and domains |
Pfam
Accession |
ID |
Position in sequence |
Description |
Type |
PF00001 |
7tm_1 |
45 → 297 |
7 transmembrane receptor (rhodopsin family) |
Family |
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Sequence |
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Sequence length |
374 |
Interactions |
View interactions |
PathwaysPathway information has different metabolic/signaling pathways associated with genes. Each record is hyperlinked to a complete information page which also includes links to the KEGG/Reactome pathway database.
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Associated diseases
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Causal |
Disease name |
Disease term |
dbSNP ID |
References |
Narcolepsy |
Narcolepsy, Narcolepsy type 1 |
rs104894574, rs387906655 |
24204295, 21170044 |
Obesity |
Obesity |
rs34911341, rs74315349, rs1474810899, rs2282440, rs2491132, rs121918111, rs796065034, rs753856820, rs796065035, rs121918112, rs104894023, rs137852821, rs1580764441, rs137852822, rs137852823, rs137852824, rs13447324, rs121913562, rs121913564, rs74315393, rs121913556, rs2989924, rs193922650, rs193922685, rs193922687, rs751160202, rs1421085, rs747681609, rs1553400259, rs13447339, rs370479598, rs1554394014, rs1553174844, rs756232889, rs369841551, rs1557670950, rs1571321748, rs148538980, rs1572820988, rs1591461970, rs1419374563, rs745921568, rs144159890, rs1570714352, rs779783209, rs1573250294, rs1573254045, rs1580744791, rs1580746829, rs6548238, rs7138803, rs7754840 |
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Unknown |
Disease name |
Disease term |
dbSNP ID |
References |
Amnesia |
Amnesia, Transient Global |
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Cataplexy |
Cataplexy |
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Hallucinations |
Hallucinations |
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Narcolepsy-cataplexy syndrome |
Narcolepsy-Cataplexy Syndrome |
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21170044, 24204295 |
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