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HTR3A 5-hydroxytryptamine receptor 3A [ Homo sapiens (human) ]

Gene ID: 3359, updated on 27-Nov-2024

Summary

Official Symbol
HTR3Aprovided by HGNC
Official Full Name
5-hydroxytryptamine receptor 3Aprovided by HGNC
Primary source
HGNC:HGNC:5297
See related
Ensembl:ENSG00000166736 MIM:182139; AllianceGenome:HGNC:5297
Gene type
protein coding
RefSeq status
REVIEWED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
HTR3; 5HT3R; 5-HT-3; 5-HT3A; 5-HT3R
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 mitogen. This receptor causes fast, depolarizing responses in neurons after activation. It appears that the heteromeric combination of A and B subunits is necessary to provide the full functional features of this receptor, since either subunit alone results in receptors with very low conductance and response amplitude. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]
Expression
Biased expression in lymph node (RPKM 3.0), appendix (RPKM 1.1) and 6 other tissues See more
Orthologs
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Genomic context

See HTR3A in Genome Data Viewer
Location:
11q23.2
Exon count:
10
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 11 NC_000011.10 (113975108..113990313)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 11 NC_060935.1 (113985458..114000652)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 11 NC_000011.9 (113845830..113861035)

Chromosome 11 - NC_000011.10Genomic Context describing neighboring genes Neighboring gene ubiquitin specific peptidase 28 Neighboring gene U7 small nuclear RNA Neighboring gene H3K27ac hESC enhancer GRCh37_chr11:113744182-113744682 Neighboring gene Sharpr-MPRA regulatory region 42 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 5543 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr11:113746853-113747514 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr11:113752951-113753737 Neighboring gene NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr11:113756096-113756882 Neighboring gene ReSE screen-validated silencer GRCh37_chr11:113766496-113766696 Neighboring gene 5-hydroxytryptamine receptor 3B Neighboring gene ReSE screen-validated silencer GRCh37_chr11:113813804-113813933 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr11:113822687-113823240 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr11:113827432-113828317 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr11:113835585-113836084 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr11:113845393-113846054 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr11:113846055-113846714 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr11:113859815-113860316 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr11:113860317-113860816 Neighboring gene uncharacterized LOC124902760 Neighboring gene uncharacterized LOC124902759 Neighboring gene uncharacterized LOC124902761 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr11:113906845-113907785

Genomic regions, transcripts, and products

Expression

  • Project title: HPA RNA-seq normal tissues
  • Description: RNA-seq was performed of tissue samples from 95 human individuals representing 27 different tissues in order to determine tissue-specificity of all protein-coding genes
  • BioProject: PRJEB4337
  • Publication: PMID 24309898
  • Analysis date: Wed Apr 4 07:08:55 2018

Bibliography

GeneRIFs: Gene References Into Functions

What's a GeneRIF?

Pathways from PubChem

Interactions

Products Interactant Other Gene Complex Source Pubs Description

General gene information

Markers

Gene Ontology Provided by GOA

Component Evidence Code Pubs
located_in cleavage furrow IDA
Inferred from Direct Assay
more info
PubMed 
is_active_in neuron projection IBA
Inferred from Biological aspect of Ancestor
more info
 
is_active_in plasma membrane IBA
Inferred from Biological aspect of Ancestor
more info
 
is_active_in plasma membrane IDA
Inferred from Direct Assay
more info
PubMed 
located_in plasma membrane TAS
Traceable Author Statement
more info
 
located_in postsynaptic membrane IEA
Inferred from Electronic Annotation
more info
 
part_of serotonin-activated cation-selective channel complex IDA
Inferred from Direct Assay
more info
PubMed 
part_of serotonin-activated cation-selective channel complex IPI
Inferred from Physical Interaction
more info
PubMed 
is_active_in synapse IBA
Inferred from Biological aspect of Ancestor
more info
 
part_of transmembrane transporter complex IBA
Inferred from Biological aspect of Ancestor
more info
 

General protein information

Preferred Names
5-hydroxytryptamine receptor 3A
Names
5-hydroxytryptamine (serotonin) receptor 3A, ionotropic
5-hydroxytryptamine receptor 3
5HT3 serotonin receptor
serotonin receptor 3A
serotonin-gated ion channel receptor

NCBI Reference Sequences (RefSeq)

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RefSeqs maintained independently of Annotated Genomes

These reference sequences exist independently of genome builds. Explain

These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.

Genomic

  1. NG_013058.1 RefSeqGene

    Range
    5034..20239
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

mRNA and Protein(s)

  1. NM_000869.6NP_000860.3  5-hydroxytryptamine receptor 3A isoform b precursor

    Status: REVIEWED

    Description
    Transcript Variant: This variant (2) lacks an in-frame segment of the coding region, compared to variant 1. It encodes a shorter isoform (b), that is missing an internal segment compared to isoform a.
    Source sequence(s)
    AK304630, AP000908, BC002354
    Consensus CDS
    CCDS8365.3
    UniProtKB/Swiss-Prot
    B4DSY6, G5E986, O60854, P46098, Q7KZM7, Q99918, Q9BSZ9
    UniProtKB/TrEMBL
    B2R9S2
    Related
    ENSP00000424189.2, ENST00000504030.7
    Conserved Domains (1) summary
    TIGR00860
    Location:23472
    LIC; Cation transporter family protein
  2. NM_001161772.3NP_001155244.1  5-hydroxytryptamine receptor 3A isoform c

    See identical proteins and their annotated locations for NP_001155244.1

    Status: REVIEWED

    Description
    Transcript Variant: This variant (3) has an alternate 5' exon and lacks an in-frame segment of the coding region, compared to variant 1. It encodes a shorter isoform (c), that has a different N-terminus and is missing an internal segment compared to isoform a.
    Source sequence(s)
    AK299973, AP000908, BC002354
    Consensus CDS
    CCDS53710.1
    UniProtKB/TrEMBL
    B2R9S2
    Related
    ENSP00000299961.4, ENST00000299961.5
    Conserved Domains (3) summary
    TIGR00860
    Location:4457
    LIC; Cation transporter family protein
    pfam02931
    Location:21227
    Neur_chan_LBD; Neurotransmitter-gated ion-channel ligand binding domain
    pfam02932
    Location:234453
    Neur_chan_memb; Neurotransmitter-gated ion-channel transmembrane region
  3. NM_213621.4NP_998786.3  5-hydroxytryptamine receptor 3A isoform a precursor

    Status: REVIEWED

    Description
    Transcript Variant: This variant (1), also known as h5-HT3RL, represents the longest transcript, and encodes the longest isoform (a).
    Source sequence(s)
    AJ003078, AK304630, AP000908, CD014118
    Consensus CDS
    CCDS8366.3
    UniProtKB/TrEMBL
    B2R9S2
    Related
    ENSP00000347754.2, ENST00000355556.6
    Conserved Domains (1) summary
    TIGR00860
    Location:23504
    LIC; Cation transporter family protein

RNA

  1. NR_046363.2 RNA Sequence

    Status: REVIEWED

    Description
    Transcript Variant: This variant (4) lacks an alternate segment and an alternate exon compared to variant 1. This variant is represented as non-coding because the use of the 5'-most supported translational start codon, as used in variant 1, renders the transcript a candidate for nonsense-mediated mRNA decay (NMD).
    Source sequence(s)
    AJ003080, AK304630, AP000908, BC002354

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2024_08

The following sections contain reference sequences that belong to a specific genome build. Explain

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000011.10 Reference GRCh38.p14 Primary Assembly

    Range
    113975108..113990313
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060935.1 Alternate T2T-CHM13v2.0

    Range
    113985458..114000652
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)