Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
200909
Gene name Gene Name - the full gene name approved by the HGNC.
5-hydroxytryptamine receptor 3D
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
HTR3D
Synonyms (NCBI Gene) Gene synonyms aliases
5HT3D
Chromosome Chromosome number
3
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
3q27.1
Summary Summary of gene provided in NCBI Entrez Gene.
The protein encoded this gene belongs to the ligand-gated ion channel receptor superfamily. This gene encodes subunit D of the type 3 receptor for 5-hydroxytryptamine (serotonin), a biogenic hormone that functions as a neurotransmitter, a mitogen and a ho
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT1057259 hsa-miR-3151 CLIP-seq
MIRT1057260 hsa-miR-3689a-3p CLIP-seq
MIRT1057261 hsa-miR-3689c CLIP-seq
MIRT1057262 hsa-miR-4283 CLIP-seq
MIRT1057263 hsa-miR-4446-3p 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:0005515 Function Protein binding IPI 17392525
GO:0005886 Component Plasma membrane TAS
GO:0005887 Component Integral component of plasma membrane IBA 21873635
GO:0007165 Process Signal transduction IBA 21873635
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
610122 24004 ENSG00000186090
Protein
UniProt ID Q70Z44
Protein name 5-hydroxytryptamine receptor 3D (5-HT3-D) (5-HT3D) (Serotonin receptor 3D)
Protein function Forms serotonin (5-hydroxytryptamine/5-HT3)-activated cation-selective channel complexes, which when activated cause fast, depolarizing responses in neurons.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF02931 Neur_chan_LBD 44 151 Neurotransmitter-gated ion-channel ligand binding domain Family
PF02932 Neur_chan_memb 236 431 Neurotransmitter-gated ion-channel transmembrane region Family
Tissue specificity TISSUE SPECIFICITY: Expressed in liver, as well as fetal and adult colon and kidney. {ECO:0000269|PubMed:12801637}.
Sequence
Sequence length 454
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 information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Schizophrenia Schizophrenia rs13447324, rs387906932, rs387906933, rs863223354, rs863223355, rs776061422, rs863223349, rs748809996, rs759748655, rs863223353, rs863223350, rs863223356, rs781821239, rs863223348, rs863223346
View all (12 more)
20356718
Associations from Text Mining
Disease Name Relationship Type References
Dyspepsia Associate 21192076
Irritable Bowel Syndrome Associate 21192076
Obsessive Compulsive Disorder Associate 27616601