Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
3356
Gene name Gene Name - the full gene name approved by the HGNC.
5-hydroxytryptamine receptor 2A
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
HTR2A
Synonyms (NCBI Gene) Gene synonyms aliases
5-HT2A, HTR2
Chromosome Chromosome number
13
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
13q14.2
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes one of the receptors for serotonin, a neurotransmitter with many roles. Mutations in this gene are associated with susceptibility to schizophrenia and obsessive-compulsive disorder, and are also associated with response to the antidepres
SNPs SNP information provided by dbSNP.
SNP ID Visualize variation Clinical significance Consequence
rs7997012 A>C,G,T Drug-response, benign Intron variant
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT450850 hsa-miR-203a-3p PAR-CLIP 22100165
MIRT450849 hsa-miR-4251 PAR-CLIP 22100165
MIRT450848 hsa-miR-4329 PAR-CLIP 22100165
MIRT450847 hsa-miR-6761-5p PAR-CLIP 22100165
MIRT450846 hsa-miR-4303 PAR-CLIP 22100165
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0001587 Function Gq/11-coupled serotonin receptor activity IDA 18703043
GO:0001618 Function Virus receptor activity IEA
GO:0001659 Process Temperature homeostasis IEA
GO:0001965 Function G-protein alpha-subunit binding IEA
GO:0004993 Function G protein-coupled serotonin receptor activity IBA 21873635
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
182135 5293 ENSG00000102468
Protein
UniProt ID P28223
Protein name 5-hydroxytryptamine receptor 2A (5-HT-2) (5-HT-2A) (Serotonin receptor 2A)
Protein function G-protein coupled receptor for 5-hydroxytryptamine (serotonin) (PubMed:1330647, PubMed:18703043, PubMed:19057895, PubMed:21645528, PubMed:22300836, PubMed:35084960, PubMed:38552625). Also functions as a receptor for various drugs and psychoactiv
PDB 6A93 , 6A94 , 6WGT , 6WH4 , 6WHA , 7RAN , 7VOD , 7VOE , 7WC4 , 7WC5 , 7WC6 , 7WC7 , 7WC8 , 7WC9 , 8JT8 , 8UWL , 8V6U , 8ZMG
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00001 7tm_1 91 380 7 transmembrane receptor (rhodopsin family) Family
Tissue specificity TISSUE SPECIFICITY: Detected in brain cortex (at protein level). Detected in blood platelets. {ECO:0000269|PubMed:18297054}.
Sequence
Sequence length 471
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG   Reactome
  Calcium signaling pathway
Neuroactive ligand-receptor interaction
Gap junction
Serotonergic synapse
Inflammatory mediator regulation of TRP channels
  Serotonin receptors
G alpha (q) signalling events
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Autism Autistic Disorder rs121964908, rs62643608, rs181327458, rs797046134, rs869312704, rs1555013332, rs876657679, rs1057518999, rs1057518658, rs771827120, rs1555187899, rs773080572, rs753871454, rs1684130791, rs1684180699
View all (8 more)
17280648
Migraine Cervical Migraine Syndrome, Migraine Disorders rs794727411 12482207
Obesity Obesity rs74315349, rs1474810899, rs121918111, rs796065034, rs753856820, rs796065035, rs121918112, rs104894023, rs137852821, rs1580764441, rs137852822, rs137852823, rs137852824, rs13447324, rs121913562
View all (27 more)
17097612
Schizophrenia Schizophrenia rs13447324, rs387906932, rs387906933, rs863223354, rs863223355, rs776061422, rs863223349, rs748809996, rs759748655, rs863223353, rs863223350, rs863223356, rs781821239, rs863223348, rs863223346
View all (12 more)
14708030, 18513383
Unknown
Disease term Disease name Evidence References Source
Chronic obstructive pulmonary disease Chronic Obstructive Airway Disease 22048642 ClinVar
Mental depression Mental Depression, Depressive disorder, Major depression, single episode, Unipolar Depression, Major Depressive Disorder 25106036, 24314147, 23537781, 23973249, 23158458, 24411530, 19758789, 24801750, 24962835, 25270656, 22612784, 25108775 ClinVar
Metabolic diseases Metabolic Diseases 19142110 ClinVar
Neuroblastoma Neuroblastoma Loss of SNAI2 function reduces self-renewal, 3D invasion as well as metastatic spread in vivo, while strongly sensitizing neuroblastoma cells to RA-induced growth inhibition. GWAS, CBGDA
Associations from Text Mining
Disease Name Relationship Type References
Acute Coronary Syndrome Associate 33582601
Akathisia Drug Induced Associate 38377518
Alcoholism Associate 11287798, 17713649
Alzheimer Disease Associate 16640790, 17525976, 26303700, 34336000
Anorexia Nervosa Associate 16087994, 20545463
Antisocial Personality Disorder Associate 36094569
Anxiety Associate 23397970, 25041420, 29249830
Anxiety Disorders Associate 37984468
Arthritis Rheumatoid Associate 16699051, 20179740, 23254357, 36561742
Asthma Associate 37238670