The SLC25A15 gene homepage

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 NG_012248.1
Transcript reference NM_014252.3
Exon/intron information NM_014252.3 exon/intron table
Associated with diseases ID, hyperornithinemia-hyperammonemia-homocitrullinemia syndrome (HHH)
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 52
Unique public DNA variants reported 34
Individuals with public variants 33
Hidden variants 5
Download all this gene's data Download all data
Notes Establishment of this gene variant database (LSDB) was supported by the Leiden University Medical Center (LUMC), Leiden, Nederland.
Date created March 20, 2009
Date last updated September 17, 2021
Version SLC25A15:210917

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
Reading frame checker The Reading-frame checker generates a prediction of the effect of whole-exon changes. Active for: NM_014252.3.
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
Homepage URL
HGNC 10985
Entrez Gene 10166
PubMed articles SLC25A15
OMIM - Gene 603861
OMIM - Diseases hyperornithinemia-hyperammonemia-homocitrullinemia syndrome (HHH)
GeneCards SLC25A15
GeneTests SLC25A15
Orphanet SLC25A15

Active transcripts




NCBI ID     

NCBI Protein ID     

00019197 13 solute carrier family 25 (mitochondrial carrier; ornithine transporter) member 15 NM_014252.3 NP_055067.1 52

Copyright & disclaimer
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