Chromosome 19 Open Reading Frame 12 (C19orf12)

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Chromosome 19 Open Reading Frame 12 (C19orf12)
The finished human chromosome 19 sequence, comprising a gene density more than double the genome-wide average1, 2, marks the culmination of 18 yr of research spanning the history of modern genomics.
The Department of Energy's (DOE) role in the project was initiated through an effort to understand how the body responds to and repairs radiation damage3, 4. A link between unrepaired DNA damage and human cancer5, and the subsequent mapping of multiple DNA repair genes to the chromosome6, provided the impetus for the DOE to select the chromosome as one of its sequencing targets7. The physical mapping was completed at Lawrence Livermore National Laboratory (LLNL) in 1995 with the generation of the first high-quality metric map of a human chromosome8.

Organism species: Homo sapiens (Human)

CATALOG NO. PRODUCT NAME APPLICATIONS
Proteins n/a Recombinant Chromosome 19 Open Reading Frame 12 (C19orf12) Recombinant Protein Customized Service Offer
Antibodies n/a Monoclonal Antibody to Chromosome 19 Open Reading Frame 12 (C19orf12) Monoclonal Antibody Customized Service Offer
n/a Polyclonal Antibody to Chromosome 19 Open Reading Frame 12 (C19orf12) Polyclonal Antibody Customized Service Offer
Assay Kits n/a CLIA Kit for Chromosome 19 Open Reading Frame 12 (C19orf12) CLIA Kit Customized Service Offer
n/a ELISA Kit for Chromosome 19 Open Reading Frame 12 (C19orf12) ELISA Kit Customized Service Offer

Organism species: Mus musculus (Mouse)

CATALOG NO. PRODUCT NAME APPLICATIONS
Proteins n/a Recombinant Chromosome 19 Open Reading Frame 12 (C19orf12) Recombinant Protein Customized Service Offer
Antibodies n/a Monoclonal Antibody to Chromosome 19 Open Reading Frame 12 (C19orf12) Monoclonal Antibody Customized Service Offer
n/a Polyclonal Antibody to Chromosome 19 Open Reading Frame 12 (C19orf12) Polyclonal Antibody Customized Service Offer
Assay Kits n/a CLIA Kit for Chromosome 19 Open Reading Frame 12 (C19orf12) CLIA Kit Customized Service Offer
n/a ELISA Kit for Chromosome 19 Open Reading Frame 12 (C19orf12) ELISA Kit Customized Service Offer

Organism species: Rattus norvegicus (Rat)

CATALOG NO. PRODUCT NAME APPLICATIONS
Proteins n/a Recombinant Chromosome 19 Open Reading Frame 12 (C19orf12) Recombinant Protein Customized Service Offer
Antibodies n/a Monoclonal Antibody to Chromosome 19 Open Reading Frame 12 (C19orf12) Monoclonal Antibody Customized Service Offer
n/a Polyclonal Antibody to Chromosome 19 Open Reading Frame 12 (C19orf12) Polyclonal Antibody Customized Service Offer
Assay Kits n/a CLIA Kit for Chromosome 19 Open Reading Frame 12 (C19orf12) CLIA Kit Customized Service Offer
n/a ELISA Kit for Chromosome 19 Open Reading Frame 12 (C19orf12) ELISA Kit Customized Service Offer
  1. "Complete sequencing and characterization of 21,243 full-length human cDNAs." Nat. Genet. 36:40-45(2004) [PubMed] [Europe PMC] [Abstract]
  2. "The DNA sequence and biology of human chromosome 19." Nature 428:529-535(2004) [PubMed] [Europe PMC] [Abstract]
  3. "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]
  4. "The full-ORF clone resource of the German cDNA consortium."BMC Genomics 8:399-399(2007) [PubMed] [Europe PMC] [Abstract]
  5. "A novel frameshift mutation of C19ORF12 causes NBIA4 with cerebellar atrophy and manifests with severe peripheral motor axonal neuropathy."Clin. Genet. 85:290-292(2014) [PubMed] [Europe PMC] [Abstract]
  6. "Absence of an orphan mitochondrial protein, c19orf12, causes a distinct clinical subtype of neurodegeneration with brain iron accumulation." Am. J. Hum. Genet. 89:543-550(2011) [PubMed] [Europe PMC] [Abstract]
  7. "C19orf12 mutations in neurodegeneration with brain iron accumulation mimicking juvenile amyotrophic lateral sclerosis."J. Neurol. 259:2434-2439(2012) [PubMed] [Europe PMC] [Abstract]
  8. "A new phenotype of brain iron accumulation with dystonia, optic atrophy, and peripheral neuropathy." Mov. Disord. 27:789-793(2012) [PubMed] [Europe PMC] [Abstract]
  9. "New NBIA subtype: genetic, clinical, pathologic, and radiographic features of MPAN." Neurology 80:268-275(2013) [PubMed] [Europe PMC] [Abstract]
  10. "Hereditary spastic paraplegia type 43 (SPG43) is caused by mutation in C19orf12." Hum. Mutat. 34:1357-1360(2013) [PubMed] [Europe PMC] [Abstract]