SLC19A2 gene homepage

MSeqDR-LSDB: Mitochondrial Disease LSDB
General information
Gene symbol SLC19A2
Gene name solute carrier family 19 (thiamine transporter), member 2
Chromosome 1
Chromosomal band q23.3
Imprinted Unknown
Genomic reference NC_000001.10
Transcript reference NM_006996.2
Associated with diseases -
Citation reference(s) -
Curators (0) -
Total number of public variants reported 5
Unique public DNA variants reported 5
Individuals with public variants 0
Hidden variants 0
Download all this gene's data Download all data
Notes MSeqDR-LSDB
Date created November 12, 2013

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
UCSC Genome Browser Show variants in the UCSC Genome Browser (full view, compact view)
Ensembl Genome Browser Show variants in the Ensembl Genome Browser (full view, compact view)
NCBI Sequence Viewer Show distribution histogram of variants in the NCBI Sequence Viewer

Links to other resources
HGNC 10938
Entrez Gene 10560
PubMed articles SLC19A2
OMIM - Gene 603941
HGMD SLC19A2
GeneCards SLC19A2
GeneTests SLC19A2


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00001143 1 solute carrier family 19 (thiamine transporter), member 2 NM_006996.2 NP_008927.1 5


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Mitochondrial Disease Sequence Data Resource (MSeqDR) Consortium