Porcupine Homolog (PORCN)

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MG61; PORC; PPN; por; Protein-cysteine N-palmitoyltransferase porcupine

Porcupine Homolog (PORCN)
PORCN has 5 transcript variants that encode 5 protein isoforms with tissue-specific variability and expression (PORCA-PROCE). To investigate how developmental expression of PORCN contributes to the specific defects in focal dermal hypoplasia (FDH), Wang et al. (2007) performed RNA in situ hybridization on embryonic day 12.5 and embryonic day 14.5 mouse embryos using a probe that detects all known mouse Porcn transcript variants. They detected Porcn and the distinctive peripheral pattern in cartilage primordia of long bones and digits, calvarian, facial skeleton, molar tooth bud, and the petrous part of the temporal bone. They also observed it in developing skin of the anterior body wall and limbs and at lower levels in developing cerebral cortex and retina.

Organism species: Homo sapiens (Human)

CATALOG NO. PRODUCT NAME APPLICATIONS
Proteins n/a Recombinant Porcupine Homolog (PORCN) Recombinant Protein Customized Service Offer
Antibodies n/a Monoclonal Antibody to Porcupine Homolog (PORCN) Monoclonal Antibody Customized Service Offer
n/a Polyclonal Antibody to Porcupine Homolog (PORCN) Polyclonal Antibody Customized Service Offer
Assay Kits n/a CLIA Kit for Porcupine Homolog (PORCN) CLIA Kit Customized Service Offer
n/a ELISA Kit for Porcupine Homolog (PORCN) ELISA Kit Customized Service Offer

Organism species: Mus musculus (Mouse)

CATALOG NO. PRODUCT NAME APPLICATIONS
Proteins n/a Recombinant Porcupine Homolog (PORCN) Recombinant Protein Customized Service Offer
Antibodies n/a Monoclonal Antibody to Porcupine Homolog (PORCN) Monoclonal Antibody Customized Service Offer
n/a Polyclonal Antibody to Porcupine Homolog (PORCN) Polyclonal Antibody Customized Service Offer
Assay Kits n/a CLIA Kit for Porcupine Homolog (PORCN) CLIA Kit Customized Service Offer
n/a ELISA Kit for Porcupine Homolog (PORCN) ELISA Kit Customized Service Offer

Organism species: Rattus norvegicus (Rat)

CATALOG NO. PRODUCT NAME APPLICATIONS
Proteins n/a Recombinant Porcupine Homolog (PORCN) Recombinant Protein Customized Service Offer
Antibodies n/a Monoclonal Antibody to Porcupine Homolog (PORCN) Monoclonal Antibody Customized Service Offer
n/a Polyclonal Antibody to Porcupine Homolog (PORCN) Polyclonal Antibody Customized Service Offer
Assay Kits n/a CLIA Kit for Porcupine Homolog (PORCN) CLIA Kit Customized Service Offer
n/a ELISA Kit for Porcupine Homolog (PORCN) ELISA Kit Customized Service Offer
  1. "Molecular cloning and initial characterization of the MG61/PORC gene, the human homologue of the Drosophila segment polarity gene Porcupine."Gene 288:147-157(2002) [PubMed] [Europe PMC] [Abstract]
  2. "Complete sequencing and characterization of 21,243 full-length human cDNAs." Nat. Genet. 36:40-45(2004) [PubMed] [Europe PMC] [Abstract]
  3. "The DNA sequence of the human X chromosome." Nature 434:325-337(2005) [PubMed] [Europe PMC] [Abstract]
  4. "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]
  5. "Deficiency of PORCN, a regulator of Wnt signaling, is associated with focal dermal hypoplasia."Nat. Genet. 39:833-835(2007) [PubMed] [Europe PMC] [Abstract]
  6. "WLS-dependent secretion of WNT3A requires Ser209 acylation and vacuolar acidification."J. Cell Sci. 123:3357-3367(2010) [PubMed] [Europe PMC] [Abstract]
  7. "Single-cell imaging of Wnt palmitoylation by the acyltransferase porcupine."Nat. Chem. Biol. 10:61-68(2014) [PubMed] [Europe PMC] [Abstract]
  8. "Mutations in X-linked PORCN, a putative regulator of Wnt signaling, cause focal dermal hypoplasia."Nat. Genet. 39:836-838(2007) [PubMed] [Europe PMC] [Abstract]
  9. "Three novel mutations in the PORCN gene underlying focal dermal hypoplasia."Clin. Genet. 73:373-379(2008) [PubMed] [Europe PMC] [Abstract]
  10. "Novel PORCN mutations in focal dermal hypoplasia."Clin. Genet. 76:535-543(2009) [PubMed] [Europe PMC] [Abstract]
  11. "Goltz-Gorlin (focal dermal hypoplasia) and the microphthalmia with linear skin defects (MLS) syndrome: no evidence of genetic overlap."Eur. J. Hum. Genet. 17:1207-1215(2009) [PubMed] [Europe PMC] [Abstract]
  12. "PORCN mutations in focal dermal hypoplasia: coping with lethality." Hum. Mutat. 30:E618-E628(2009) [PubMed] [Europe PMC] [Abstract]
  13. "Phenotype and genotype in 17 patients with Goltz-Gorlin syndrome."J. Med. Genet. 46:716-720(2009) [PubMed] [Europe PMC] [Abstract]
  14. "Mutation update for the PORCN gene."Hum. Mutat. 32:723-728(2011) [PubMed] [Europe PMC] [Abstract]