View SLC19A2 gene homepage

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 NG_008255.1
Transcript reference NM_006996.2
Associated with diseases Megaloblastic anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness
Citation reference(s) -
Curators (1) LOVD-team, but with Curator vacancy
Total number of public variants reported 3
Unique public DNA variants reported 3
Individuals with public variants 3
Hidden variants 0
Date created May 03, 2013
Date last updated April 02, 2015
Version SLC19A2:150402

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
OMIM - Diseases Megaloblastic anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00019147 1 solute carrier family 19 (thiamine transporter), member 2 NM_006996.2 NP_008927.1 3