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
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 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


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Mitochondrial Disease Sequence Data Resource (MSeqDR) Consortium

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