SLC19A3 gene homepage

MSeqDR-LSDB: Mitochondrial Disease LSDB
General information
Gene symbol SLC19A3
Gene name solute carrier family 19 (thiamine transporter), member 3
Chromosome 2
Chromosomal band q37
Imprinted Unknown
Genomic reference NC_000002.11
Transcript reference NM_025243.3, XM_005246871.1, XM_005246872.1, XM_005246873.1, XM_005246874.1, XM_005246875.1
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
Date created November 07, 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 16266
Entrez Gene 80704
PubMed articles SLC19A3
OMIM - Gene 606152
GeneCards SLC19A3
GeneTests SLC19A3

Active transcripts




NCBI ID     

NCBI Protein ID     

00000296 2 transcript variant X1 XM_005246871.1 XP_005246928.1 5
00000297 2 solute carrier family 19 (thiamine transporter), member 3 NM_025243.3 NP_079519.1 5
00000298 2 transcript variant X4 XM_005246874.1 XP_005246931.1 5
00000299 2 transcript variant X3 XM_005246873.1 XP_005246930.1 5
00000300 2 transcript variant X2 XM_005246872.1 XP_005246929.1 5
00000301 2 transcript variant X5 XM_005246875.1 XP_005246932.1 5

Copyright & disclaimer
Sources: GeneDX

Mitochondrial Disease Sequence Data Resource (MSeqDR) Consortium