LOVD SLC19A2 homepage

General information
Gene name solute carrier family 19 (thiamine transporter), member 2
Gene symbol SLC19A2
Chromosome Location 1q23.3
Database location EURO-WABB Project
Curator Dewi Astuti and Professor Timothy Barrett
Database reference for citations Astuti et al., 2017
PubMed references View all (unique) PubMed references in the SLC19A2 database
Date of creation May 25, 2011
Last update April 05, 2017
Version SLC19A2 170405
Add sequence variant Submit a sequence variant
First time submitters Register here
Reference sequence file Genomic reference sequence for describing sequence variants
Genomic refseq ID NG_008255.1
Transcript refseq ID NM_006996.2
Exon/intron information Exon/intron information table
Total number of unique DNA variants reported 48
Total number of individuals with variant(s) 82
Total number of variants reported 156
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Graphical displays and utilities
Summary tables Summary of all sequence variants in the SLC19A2 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 SLC19A2 database, without patient data
Complete sequence variant listing Listing of all sequence variants in the SLC19A2 database
Variants with no known pathogenicity Listing of all SLC19A2 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 10938
Entrez Gene 10560
OMIM - Gene 603941
OMIM - Disease Thiamine-Responsive Megaloblastic Anemia Syndrome
UniProtKB (SwissProt/TrEMBL) O60779
GeneCards SLC19A2
GeneTests SLC19A2

Copyright & disclaimer
The contents of this LOVD database are the intellectual property of the respective curator(s). Any unauthorised use, copying, storage or distribution of this material without written permission from the curator(s) will lead to copyright infringement with possible ensuing litigation. Copyright © 2018. All Rights Reserved. For further details, refer to Directive 96/9/EC of the European Parliament and the Council of March 11 (1996) on the legal protection of databases.

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