View 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 0
Unique public DNA variants reported 0
Individuals with public variants 0
Hidden variants 0
Notes MSeqDR-LSDB
Date created November 07, 2013

Links to other resources
HGNC 16266
Entrez Gene 80704
PubMed articles SLC19A3
OMIM - Gene 606152
HGMD SLC19A3
GeneCards SLC19A3
GeneTests SLC19A3


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00000296 2 transcript variant X1 XM_005246871.1 XP_005246928.1 0
00000297 2 solute carrier family 19 (thiamine transporter), member 3 NM_025243.3 NP_079519.1 0
00000298 2 transcript variant X4 XM_005246874.1 XP_005246931.1 0
00000299 2 transcript variant X3 XM_005246873.1 XP_005246930.1 0
00000300 2 transcript variant X2 XM_005246872.1 XP_005246929.1 0
00000301 2 transcript variant X5 XM_005246875.1 XP_005246932.1 0


Copyright & disclaimer
Sources: GeneDX http://www.genedx.com

Mitochondrial Disease Sequence Data Resource (MSeqDR) Consortium