By sequencing YAC clones containing a CpG island in the Prader-Willi syndrome (PWS) critical region on chromosome 15, followed by database analysis and PCR and 3-prime RACE of a human testis cDNA library, Farber et al. (2000) cloned C15ORF2. The deduced protein contains 1,156 amino acids. Northern blot analysis detected a 7.5-kb transcript in adult testis, but not in fetal testis or in any other adult or fetal tissues examined. Southern blot analysis detected C15ORF2 in several primates, but not in any other mammalian or avian species examined. The primate sequences share between 97 and 99% identities. Farber et al. (2000) found that a CpG island associated with C15ORF2 was methylated in all tissues tested except for germ cells. Although C15ORF2 maps between the imprinted genes MAGEL2 and SNRPN , they demonstrated that C15ORF2 was biallelically expressed in adult testis.
Organism species: Homo sapiens (Human)
CATALOG NO. | PRODUCT NAME | APPLICATIONS | |
Proteins | n/a | Recombinant Nuclear Pore Associated Protein 1 (NPAP1) | Recombinant Protein Customized Service Offer |
Antibodies | n/a | Monoclonal Antibody to Nuclear Pore Associated Protein 1 (NPAP1) | Monoclonal Antibody Customized Service Offer |
n/a | Polyclonal Antibody to Nuclear Pore Associated Protein 1 (NPAP1) | Polyclonal Antibody Customized Service Offer | |
Assay Kits | n/a | CLIA Kit for Nuclear Pore Associated Protein 1 (NPAP1) | CLIA Kit Customized Service Offer |
n/a | ELISA Kit for Nuclear Pore Associated Protein 1 (NPAP1) | ELISA Kit Customized Service Offer |
- "Identification of a testis-specific gene (c15orf2) in the Prader-Willi syndrome region on chromosome 15."Genomics 65:174-183(2000) [PubMed] [Europe PMC] [Abstract]
- "Analysis of the DNA sequence and duplication history of human chromosome 15." Nature 440:671-675(2006) [PubMed] [Europe PMC] [Abstract]
- "The consensus coding sequences of human breast and colorectal cancers." Science 314:268-274(2006) [PubMed] [Europe PMC] [Abstract]
- "C15orf2 and a novel noncoding transcript from the Prader-Willi/Angelman syndrome region show monoallelic expression in fetal brain."Genomics 89:588-595(2007) [PubMed] [Europe PMC] [Abstract]
- "The C15orf2 gene in the Prader-Willi syndrome region is subject to genomic imprinting and positive selection."Neurogenetics 11:153-161(2010) [PubMed] [Europe PMC] [Abstract]
- "The imprinted NPAP1/C15orf2 gene in the Prader-Willi syndrome region encodes a nuclear pore complex associated protein."Hum. Mol. Genet. 21:4038-4048(2012) [PubMed] [Europe PMC] [Abstract]