SLC25A15 gene homepage

MSeqDR-LSDB: Mitochondrial Disease LSDB
General information
Gene symbol SLC25A15
Gene name solute carrier family 25 (mitochondrial carrier; ornithine transporter) member 15
Chromosome 13
Chromosomal band q14
Imprinted Unknown
Genomic reference NC_000013.10
Transcript reference NM_014252.3, XM_005266210.1
Associated with diseases 238970
Citation reference(s) -
Curators (0) -
Total number of public variants reported 99
Unique public DNA variants reported 81
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 10985
Entrez Gene 10166
PubMed articles SLC25A15
OMIM - Gene 603861
OMIM - Diseases 238970 (Hyperornithinemia-hyperammonemia-homocitrullinemia syndrome, 238970 (3))
GeneCards SLC25A15
GeneTests SLC25A15

Active transcripts




NCBI ID     

NCBI Protein ID     

00001152 13 solute carrier family 25 (mitochondrial carrier; ornithine transporter) member 15 NM_014252.3 NP_055067.1 99
00001153 13 transcript variant X1 XM_005266210.1 XP_005266267.1 87

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Mitochondrial Disease Sequence Data Resource (MSeqDR) Consortium