LOVD STXBP2 homepage

General information
Gene name syntaxin binding protein 2
Gene symbol STXBP2
Chromosome Location 19p13.3-p13.2
Database location https://research.cchmc.org/LOVD2/
Curator Ammar Husami
PubMed references View all (unique) PubMed references in the STXBP2 database
Date of creation April 30, 2010
Last update May 06, 2010
Version STXBP2 100506
Add sequence variant Submit a sequence variant
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Reference sequence file coding DNA reference sequence for describing sequence variants
Genomic refseq ID NG_016709.1
Transcript refseq ID NM_006949.2
Exon/intron information Exon/intron information table
Total number of unique DNA variants reported 20
Total number of individuals with variant(s) 2
Total number of variants reported 20
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Graphical displays and utilities
Summary tables Summary of all sequence variants in the STXBP2 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 STXBP2 database, without patient data
Complete sequence variant listing Listing of all sequence variants in the STXBP2 database
Variants with no known pathogenicity Listing of all STXBP2 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 11445
Entrez Gene 6813
OMIM - Gene 601717
UniProtKB (SwissProt/TrEMBL) Q15833
HGMD STXBP2
GeneCards STXBP2
GeneTests STXBP2