SLC7A9 gene homepage

MSeqDR-LSDB: Mitochondrial Disease LSDB
General information
Gene symbol SLC7A9
Gene name solute carrier family 7 (amino acid transporter light chain, bo,+ system), member 9
Chromosome 19
Chromosomal band q13.11
Imprinted Unknown
Genomic reference NC_000019.9
Transcript reference NM_001126335.1, NM_014270.4
Associated with diseases -
Citation reference(s) -
Curators (0) -
Total number of public variants reported 10
Unique public DNA variants reported 10
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 11067
Entrez Gene 11136
PubMed articles SLC7A9
OMIM - Gene 604144
HGMD SLC7A9
GeneCards SLC7A9
GeneTests SLC7A9


Active transcripts


ID     
Chr     
Name     
NCBI ID     
NCBI Protein ID     
DescendingVariants     
00001192 19 solute carrier family 7 (glycoprotein-associated amino acid transporter light chain, bo,+ system), member 9, transcript variant 2 NM_001126335.1 NP_001119807.1 10
00001193 19 solute carrier family 7 (glycoprotein-associated amino acid transporter light chain, bo,+ system), member 9, transcript variant 1 NM_014270.4 NP_055085.1 10


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Mitochondrial Disease Sequence Data Resource (MSeqDR) Consortium

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