SLC25A13 gene homepage

MSeqDR-LSDB: Mitochondrial Disease LSDB
General information
Gene symbol SLC25A13
Gene name solute carrier family 25 (aspartate/glutamate carrier), member 13
Chromosome 7
Chromosomal band q21.3
Imprinted Unknown
Genomic reference NC_000007.13
Transcript reference NM_001160210.1, NM_014251.2, NR_027662.1
Associated with diseases 605814, CTLN2
Citation reference(s) -
Curators (0) -
Total number of public variants reported 47
Unique public DNA variants reported 29
Individuals with public variants 0
Hidden variants 0
Download all this gene's data Download all data
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 10983
Entrez Gene 10165
PubMed articles SLC25A13
OMIM - Gene 603859
OMIM - Diseases 605814 (Citrullinemia, type II, neonatal-onset, 605814 (3))
CTLN2 (Citrullinemia, adult-onset type II, 603471 (3))
GeneCards SLC25A13
GeneTests SLC25A13

Active transcripts




NCBI ID     

NCBI Protein ID     

00001150 7 solute carrier family 25, member 13 (citrin), transcript variant 2 NM_014251.2 NP_055066.1 47
00001149 7 solute carrier family 25, member 13 (citrin), transcript variant 3 NR_027662.1 - 45
00001151 7 solute carrier family 25, member 13 (citrin), transcript variant 1 NM_001160210.1 NP_001153682.1 45

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Mitochondrial Disease Sequence Data Resource (MSeqDR) Consortium