LOVD HTR3B homepage

General information
Gene name 5-hydroxytryptamine (serotonin) receptor 3B
Gene symbol HTR3B
Chromosome Location 11q23.1
Database location University of Heidelberg
Curator Beate Niesler
PubMed references View all (unique) PubMed references in the HTR3B database
Date of creation May 25, 2010
Last update June 28, 2016
Version HTR3B160628
Add sequence variant Submit a sequence variant
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Reference sequence file Genomic reference sequence for describing sequence variants
Genomic refseq ID NG_011483.1
Transcript refseq ID NM_006028.4
Exon/intron information Exon/intron information table
Total number of unique DNA variants reported 22
Total number of individuals with variant(s) 53
Total number of variants reported 53
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NOTE The transcript reference sequence version has been recently updated (from v3 to v4). We are currently updating the data in this database to match the new version. Please be patient.

Graphical displays and utilities
Summary tables Summary of all sequence variants in the HTR3B database, sorted by type of variant (with graphical displays and statistics)
Reading-frame checker The Reading-frame checker generates a prediction of the effect of whole-exon changes
UCSC Genome Browser Show variants in the UCSC Genome Browser (compact view)
Ensembl Genome Browser Show variants in the Ensembl Genome Browser (compact view)
NCBI Sequence Viewer Show distribution histogram of variants in the NCBI Sequence Viewer

Sequence variant tables
Unique sequence variants Listing of all unique sequence variants in the HTR3B database, without patient data
Complete sequence variant listing Listing of all sequence variants in the HTR3B database
Variants with no known pathogenicity Listing of all HTR3B variants reported to have no noticeable phenotypic effect (note: excluding variants of unknown effect)

Search the database
By type of variant View all sequence variants of a certain type
Simple search Query the database by selecting the most important variables (exon number, type of variant, disease phenotype)
Advanced search Query the database by selecting a combination of variables
Based on patient origin View all variants based on your patient origin search terms

Links to other resources
HGNC 5298
Entrez Gene 9177
OMIM - Gene 604654
UniProtKB (SwissProt/TrEMBL) O95264
External link #1 IUPHAR/BPS
External link #2 Exome Variant Server
External link #3 ExAC
External link #4 Rome Foundation
External link #5 DSM-V

Copyright & disclaimer
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