Ornithine Transporter 1, Mitochondrial (ORNT1)

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SLC25A15; HHH; ORC1; Solute Carrier Family 25 Member 15

Ornithine Transporter 1, Mitochondrial (ORNT1)
ORNT1 transports ornithine across the inner mitochondrial membrane from the cytosol to the mitochondrial matrix. The protein is an essential component of the urea cycle, and functions in ammonium detoxification and biosynthesis of the amino acid arginine. Mutations in this gene result in hyperornithinemia-hyperammonemia-homocitrullinuria (HHH) syndrome. There is a pseudogene of this locus on the Y chromosome. The protein has 3 repeats of about 100 amino acids and each repeat has 2 predicted transmembrane alpha-helices separated by a hydrophilic segment. Northern blot analysis detected a 4.2-kb mRNA transcript in liver and pancreas, with little expression in all other tissues. In mice, the expressed protein localized to liver mitochondria and varied with changes in dietary protein.

Organism species: Homo sapiens (Human)

CATALOG NO. PRODUCT NAME APPLICATIONS
Proteins RPE465Hu01 Recombinant Ornithine Transporter 1, Mitochondrial (ORNT1) Positive Control; Immunogen; SDS-PAGE; WB.
Antibodies n/a Monoclonal Antibody to Ornithine Transporter 1, Mitochondrial (ORNT1) Monoclonal Antibody Customized Service Offer
n/a Polyclonal Antibody to Ornithine Transporter 1, Mitochondrial (ORNT1) Polyclonal Antibody Customized Service Offer
Assay Kits n/a CLIA Kit for Ornithine Transporter 1, Mitochondrial (ORNT1) CLIA Kit Customized Service Offer
n/a ELISA Kit for Ornithine Transporter 1, Mitochondrial (ORNT1) ELISA Kit Customized Service Offer

Organism species: Mus musculus (Mouse)

CATALOG NO. PRODUCT NAME APPLICATIONS
Proteins n/a Recombinant Ornithine Transporter 1, Mitochondrial (ORNT1) Recombinant Protein Customized Service Offer
Antibodies n/a Monoclonal Antibody to Ornithine Transporter 1, Mitochondrial (ORNT1) Monoclonal Antibody Customized Service Offer
n/a Polyclonal Antibody to Ornithine Transporter 1, Mitochondrial (ORNT1) Polyclonal Antibody Customized Service Offer
Assay Kits n/a CLIA Kit for Ornithine Transporter 1, Mitochondrial (ORNT1) CLIA Kit Customized Service Offer
n/a ELISA Kit for Ornithine Transporter 1, Mitochondrial (ORNT1) ELISA Kit Customized Service Offer

Organism species: Rattus norvegicus (Rat)

CATALOG NO. PRODUCT NAME APPLICATIONS
Proteins n/a Recombinant Ornithine Transporter 1, Mitochondrial (ORNT1) Recombinant Protein Customized Service Offer
Antibodies n/a Monoclonal Antibody to Ornithine Transporter 1, Mitochondrial (ORNT1) Monoclonal Antibody Customized Service Offer
n/a Polyclonal Antibody to Ornithine Transporter 1, Mitochondrial (ORNT1) Polyclonal Antibody Customized Service Offer
Assay Kits n/a CLIA Kit for Ornithine Transporter 1, Mitochondrial (ORNT1) CLIA Kit Customized Service Offer
n/a ELISA Kit for Ornithine Transporter 1, Mitochondrial (ORNT1) ELISA Kit Customized Service Offer
  1. "Hyperornithinaemia-hyperammonaemia-homocitrullinuria syndrome is caused by mutations in a gene encoding a mitochondrial ornithine transporter."Nat. Genet. 22:151-158(1999) [PubMed] [Europe PMC] [Abstract]
  2. "The mitochondrial ornithine transporter. Bacterial expression, reconstitution, functional characterization, and tissue distribution of two human isoforms."J. Biol. Chem. 278:32778-32783(2003) [PubMed] [Europe PMC] [Abstract]
  3. "Large-scale cDNA transfection screening for genes related to cancer development and progression." Proc. Natl. Acad. Sci. U.S.A. 101:15724-15729(2004) [PubMed] [Europe PMC] [Abstract]
  4. "The DNA sequence and analysis of human chromosome 13." Nature 428:522-528(2004) [PubMed] [Europe PMC] [Abstract]
  5. "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)."Genome Res. 14:2121-2127(2004) [PubMed] [Europe PMC] [Abstract]
  6. "An enzyme assisted RP-RPLC approach for in-depth analysis of human liver phosphoproteome."J. Proteomics 96:253-262(2014) [PubMed] [Europe PMC] [Abstract]
  7. "Three novel mutations (G27E, insAAC, R179X) in the ORNT1 gene of Japanese patients with hyperornithinemia, hyperammonemia, and homocitrullinuria syndrome."Ann. Neurol. 47:625-631(2000) [PubMed] [Europe PMC] [Abstract]
  8. "Seven novel mutations in the ORNT1 gene (SLC25A15) in patients with hyperornithinemia, hyperammonemia, and homocitrullinuria syndrome."Hum. Mutat. 18:460-460(2001) [PubMed] [Europe PMC] [Abstract]
  9. "Clinical and molecular findings in hyperornithinemia-hyperammonemia-homocitrullinuria syndrome."Neurology 57:911-914(2001) [PubMed] [Europe PMC] [Abstract]
  10. "A novel mutation, P126R, in a Japanese patient with HHH syndrome."Pediatr. Neurol. 26:65-67(2002) [PubMed] [Europe PMC] [Abstract]
  11. "HHH syndrome (hyperornithinaemia, hyperammonaemia, homocitrullinuria), with fulminant hepatitis-like presentation."J. Inherit. Metab. Dis. 29:186-189(2006) [PubMed] [Europe PMC] [Abstract]
  12. "Identification of novel mutations in the SLC25A15 gene in hyperornithinemia-hyperammonemia-homocitrullinuria (HHH) syndrome: a clinical, molecular, and functional study." Hum. Mutat. 30:741-748(2009) [PubMed] [Europe PMC] [Abstract]