View SLC3A1 gene homepage

MSeqDR-LSDB: Mitochondrial Disease LSDB
General information
Gene symbol SLC3A1
Gene name solute carrier family 3 (amino acid transporter heavy chain), member 1
Chromosome 2
Chromosomal band p16.3
Imprinted Unknown
Genomic reference NC_000002.11
Transcript reference NM_000341.3
Associated with diseases -
Citation reference(s) -
Curators (0) -
Total number of public variants reported 8
Unique public DNA variants reported 8
Individuals with public variants 0
Hidden variants 0
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 11025
Entrez Gene 6519
PubMed articles SLC3A1
OMIM - Gene 104614
HGMD SLC3A1
GeneCards SLC3A1
GeneTests SLC3A1


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00001186 2 solute carrier family 3 (cystine, dibasic and neutral amino acid transporters, activator of cystine, dibasic and neutral amino acid transport), member 1 NM_000341.3 NP_000332.2 8


Copyright & disclaimer
; NuclearMitome http://www.transgenomic.com

Mitochondrial Disease Sequence Data Resource (MSeqDR) Consortium