Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
5025
Gene name Gene Name - the full gene name approved by the HGNC.
Purinergic receptor P2X 4
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
P2RX4
Synonyms (NCBI Gene) Gene synonyms aliases
P2X4, P2X4R
Chromosome Chromosome number
12
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
12q24.31
Summary Summary of gene provided in NCBI Entrez Gene.
The product of this gene belongs to the family of purinoceptors for ATP. This receptor functions as a ligand-gated ion channel with high calcium permeability. The main pharmacological distinction between the members of the purinoceptor family is the relat
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT017849 hsa-miR-335-5p Microarray 18185580
MIRT1208885 hsa-miR-1184 CLIP-seq
MIRT1208886 hsa-miR-1205 CLIP-seq
MIRT1208887 hsa-miR-1231 CLIP-seq
MIRT1208888 hsa-miR-1909 CLIP-seq
Transcription factors
Transcription factor Regulation Reference
SP1 Repression 11299224
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0001614 Function Purinergic nucleotide receptor activity IDA 9016352
GO:0001614 Function Purinergic nucleotide receptor activity IMP 11606481
GO:0001894 Process Tissue homeostasis NAS 17264311
GO:0002028 Process Regulation of sodium ion transport ISS 17785580
GO:0002931 Process Response to ischemia ISS
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
600846 8535 ENSG00000135124
Protein
UniProt ID Q99571
Protein name P2X purinoceptor 4 (P2X4) (ATP receptor) (Purinergic receptor)
Protein function ATP-gated nonselective transmembrane cation channel permeable to potassium, sodium and calcium (PubMed:9016352). CTP, but not GTP or UTP, functions as a weak affinity agonist for P2RX4 (By similarity). Activated by extracellularly released ATP,
PDB 9BQH , 9BQI , 9C48
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00864 P2X_receptor 13 379 Family
Sequence
Sequence length 388
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG   Reactome
  Calcium signaling pathway
Neuroactive ligand-receptor interaction
  Elevation of cytosolic Ca2+ levels
Platelet homeostasis
Purinergic signaling in leishmaniasis infection
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Epilepsy Epilepsy, Epilepsy, Temporal Lobe, Uncinate Epilepsy, Epilepsy, Cryptogenic, Epilepsy, Benign Psychomotor, Childhood, Epilepsy, Lateral Temporal, Awakening Epilepsy rs113994140, rs28937874, rs1589762127, rs104894166, rs28939075, rs2134001459, rs104894167, rs119488099, rs119488100, rs387906420, rs121917752, rs121918622, rs281865564, rs387907313, rs397514670
View all (165 more)
12941474, 19084381
Unknown
Disease term Disease name Evidence References Source
Schizophrenia Schizophrenia GWAS
Metabolic Syndrome Metabolic Syndrome GWAS
Diabetes Diabetes GWAS
Associations from Text Mining
Disease Name Relationship Type References
AIDS Associated Nephropathy Associate 37166584
Breast Neoplasms Associate 38259456
COVID 19 Stimulate 35091759
Death Associate 31285280
Hepatitis Alcoholic Associate 35806450
Hepatitis C Associate 35806450
Inflammation Associate 17351655, 35806450
Lung Neoplasms Associate 26491047
Multiple Sclerosis Associate 28326637
Non alcoholic Fatty Liver Disease Associate 35806450