Details for: Slc25a15
Associated with
Other Information
Genular Protein ID: 2110261969
Symbol: ORNT1_MOUSE
Name: Mitochondrial ornithine transporter 1
UniProtKB Accession Codes:
Database IDs:
Citations:
PubMed ID: 10369256
Title: Hyperornithinaemia-hyperammonaemia-homocitrullinuria syndrome is caused by mutations in a gene encoding a mitochondrial ornithine transporter.
PubMed ID: 10369256
DOI: 10.1038/9658
PubMed ID: 19287344
Title: The human and mouse SLC25A29 mitochondrial transporters rescue the deficient ornithine metabolism in fibroblasts of patients with the hyperornithinemia-hyperammonemia-homocitrullinuria (HHH) syndrome.
PubMed ID: 19287344
PubMed ID: 21183079
Title: A tissue-specific atlas of mouse protein phosphorylation and expression.
PubMed ID: 21183079
PubMed ID: 23806337
Title: SIRT5-mediated lysine desuccinylation impacts diverse metabolic pathways.
PubMed ID: 23806337
Sequence Information:
- Length: 301
- Mass: 32823
- Checksum: 36F232F781785D2B
- Sequence:
MKSNPAIQAA IDLTAGAAGG TACVLTGQPF DTMKVKMQTF PDLYRGLTDC CLKTYSQVGF RGFYKGTSPA LIANIAENSV LFMCYGFCQQ VVRKVVGLDQ QAKLSDLQNA AAGSFASAFA ALVLCPTELV KCRLQTMYEM ETSGKIAASQ NTVWSVVKEI FRKDGPLGFY HGLSSTLLRE VPGYFFFFGG YELSRSFFAS GRSKDELGPV PLMLSGGFGG ICLWLAVYPV DCIKSRIQVL SMTGKQTGLV RTFLSIVKNE GITALYSGLK PTMIRAFPAN GALFLAYEYS RKLMMNQLEA W
Database document:
This is a preview of the gene's schema. Only a few entries are kept for 'singleCellExpressions,' 'mRNAExpressions,' and other large data arrays for visualization purposes. You can zoom in with the mouse wheel for a closer view, and the text will adjust automatically if necessary. For the full schema, download it here.