Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
9177
Gene name Gene Name - the full gene name approved by the HGNC.
5-hydroxytryptamine receptor 3B
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
HTR3B
Synonyms (NCBI Gene) Gene synonyms aliases
5-HT3B
Chromosome Chromosome number
11
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
11q23.2
Summary Summary of gene provided in NCBI Entrez Gene.
The product of this gene belongs to the ligand-gated ion channel receptor superfamily. This gene encodes subunit B 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.
miRTarBase ID miRNA Experiments Reference
MIRT1057244 hsa-miR-1182 CLIP-seq
MIRT1057245 hsa-miR-129-5p CLIP-seq
MIRT1057246 hsa-miR-193a-5p CLIP-seq
MIRT1057247 hsa-miR-3194-3p CLIP-seq
MIRT1057248 hsa-miR-342-5p CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
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:0005886 Component Plasma membrane IBA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
604654 5298 ENSG00000149305
Protein
UniProt ID O95264
Protein name 5-hydroxytryptamine receptor 3B (5-HT3-B) (5-HT3B) (Serotonin receptor 3B)
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,
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF02931 Neur_chan_LBD 32 239 Neurotransmitter-gated ion-channel ligand binding domain Family
PF02932 Neur_chan_memb 246 340 Neurotransmitter-gated ion-channel transmembrane region Family
Tissue specificity TISSUE SPECIFICITY: Expressed in the brain cortex, in the caudate nucleus, the hippocampus, the thalamus and the amygdala. Detected in the kidney and testis as well as in monocytes of the spleen, small and large intestine, uterus, prostate, ovary and plac
Sequence
Sequence length 441
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
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Diabetes Type 2 diabetes or prostate cancer (pleiotropy) N/A N/A GWAS
Kidney Disease Chronic kidney disease N/A N/A GWAS
Prostate cancer Prostate cancer N/A N/A GWAS
Schizophrenia Schizophrenia N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Alcoholism Associate 19185213
Antisocial Personality Disorder Associate 19185213
Bipolar Disorder Associate 27063557
Depressive Disorder Associate 36849934
Dyspnea Associate 25948405
Heart Diseases Associate 36849934
Irritable Bowel Syndrome Associate 35800179
Major Affective Disorder 2 Associate 22832903
Motion Sickness Associate 34948773
Nausea Associate 33794950