Gene Gene information from NCBI Gene database.
Entrez ID 3359
Gene name 5-hydroxytryptamine receptor 3A
Gene symbol HTR3A
Synonyms (NCBI Gene)
5-HT-35-HT3A5-HT3R5HT3RHTR3
Chromosome 11
Chromosome location 11q23.2
Summary The product of this gene belongs to the ligand-gated ion channel receptor superfamily. This gene encodes subunit A of the type 3 receptor for 5-hydroxytryptamine (serotonin), a biogenic hormone that functions as a neurotransmitter, a hormone, and a mitoge
miRNA miRNA information provided by mirtarbase database.
37
miRTarBase ID miRNA Experiments Reference
MIRT021413 hsa-miR-9-5p Microarray 17612493
MIRT1057238 hsa-miR-3160-3p CLIP-seq
MIRT1057239 hsa-miR-4307 CLIP-seq
MIRT1057240 hsa-miR-4487 CLIP-seq
MIRT1057241 hsa-miR-4710 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
41
GO ID Ontology Definition Evidence Reference
GO:0004888 Function Transmembrane signaling receptor activity IEA
GO:0005216 Function Monoatomic ion channel activity IEA
GO:0005230 Function Extracellular ligand-gated monoatomic ion channel activity IEA
GO:0005231 Function Excitatory extracellular ligand-gated monoatomic ion channel activity IBA
GO:0005515 Function Protein binding IPI 17392525
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
182139 5297 ENSG00000166736
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
P46098
Protein name 5-hydroxytryptamine receptor 3A (5-HT3-A) (5-HT3A) (5-hydroxytryptamine receptor 3) (5-HT-3) (5-HT3R) (Serotonin receptor 3A) (Serotonin-gated ion channel receptor)
Protein function Forms serotonin (5-hydroxytryptamine/5-HT3)-activated cation-selective channel complexes, which when activated cause fast, depolarizing responses in neurons. {ECO:0000269|PubMed:10521471, ECO:0000269|PubMed:12867984, ECO:0000269|PubMed:17392525,
PDB 8AXD , 8BL8 , 8BLA , 8BLB
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF02931 Neur_chan_LBD 35 242 Neurotransmitter-gated ion-channel ligand binding domain Family
PF02932 Neur_chan_memb 249 469 Neurotransmitter-gated ion-channel transmembrane region Family
Tissue specificity TISSUE SPECIFICITY: Expressed in cerebral cortex, amygdala, hippocampus, and testis. Detected in monocytes of the spleen and tonsil, in small and large intestine, uterus, prostate, ovary and placenta. {ECO:0000269|PubMed:10521471}.
Sequence
Sequence length 478
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  Reactome
  Serotonergic synapse
Taste transduction
  Neurotransmitter receptors and postsynaptic signal transmission
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
15
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
ALZHEIMER DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
AMPHETAMINE OR RELATED ACTING SYMPATHOMIMETIC ABUSE Disgenet
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
AMPHETAMINE-RELATED DISORDERS CTD
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
AUTISTIC DISORDER CTD, Disgenet
CTD, Disgenet
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Acute Promyelocytic Leukemia Promyelocytic Leukemia BEFREE 9299238
★☆☆☆☆
Found in Text Mining only
Anorexia Nervosa Anorexia BEFREE 19741568
★☆☆☆☆
Found in Text Mining only
Anxiety Anxiety Disorder BEFREE 21420406, 22014438, 28493335
★☆☆☆☆
Found in Text Mining only
Anxiety Anxiety disorder Pubtator 21420406, 22014438, 33767348, 35800179 Associate
★☆☆☆☆
Found in Text Mining only
Anxiety Disorders Anxiety Disorder BEFREE 21420406, 22014438, 28493335
★☆☆☆☆
Found in Text Mining only
Anxiety Disorders Anxiety disorder Pubtator 21420406 Associate
★☆☆☆☆
Found in Text Mining only
Asthma Asthma Pubtator 24338226 Associate
★☆☆☆☆
Found in Text Mining only
Attention deficit hyperactivity disorder Attention Deficit Hyperactivity Disorder BEFREE 30074224
★☆☆☆☆
Found in Text Mining only
Autistic Disorder Autism BEFREE 19184136
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Autistic Disorder Autism CTD_human_DG 19184136
★★☆☆☆
Found in Text Mining + Unknown/Other Associations