Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
285242
Gene name Gene Name - the full gene name approved by the HGNC.
5-hydroxytryptamine receptor 3E
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
HTR3E
Synonyms (NCBI Gene) Gene synonyms aliases
5-HT3-E, 5-HT3E, 5-HT3c1
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.
This locus encodes a 5-hydroxytryptamine (serotonin) receptor subunit. The encoded protein, subunit E, may play a role in neurotransmission in myenteric neurons. Genes encoding subunits C, D and E form a cluster on chromosome 3. Alternatively spliced tran
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT001979 hsa-miR-510-5p Luciferase reporter assay 18614545
MIRT001979 hsa-miR-510-5p Luciferase reporter assay 18614545
MIRT001979 hsa-miR-510-5p Luciferase reporter assay 18614545
MIRT1057271 hsa-miR-1184 CLIP-seq
MIRT1057272 hsa-miR-1205 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:0005886 Component Plasma membrane TAS
GO:0005887 Component Integral component of plasma membrane IBA 21873635
GO:0007165 Process Signal transduction IBA 21873635
GO:0007210 Process Serotonin receptor signaling pathway IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
610123 24005 ENSG00000186038
Protein
UniProt ID A5X5Y0
Protein name 5-hydroxytryptamine receptor 3E (5-HT3-E) (5-HT3E) (Serotonin receptor 3E)
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 43 247 Neurotransmitter-gated ion-channel ligand binding domain Family
PF02932 Neur_chan_memb 254 428 Neurotransmitter-gated ion-channel transmembrane region Family
Tissue specificity TISSUE SPECIFICITY: Expressed in adult colon and intestine. {ECO:0000269|PubMed:12801637, ECO:0000269|PubMed:14597179}.
Sequence
Sequence length 456
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)
19794330
Associations from Text Mining
Disease Name Relationship Type References
Dyspepsia Associate 21192076
Irritable Bowel Syndrome Associate 21192076