FSHD Region Gene 2 (FRG2)
Two potential nuclear localization signals at amino acid positions 96 and 157 were predicted as well as a peroxisomal targeting signal (PTS1) at the C-terminal end of the protein.
FRG2 expression was undetectable in all tissues tested except for differentiating myoblasts of patients with facioscapulohumeral muscular dystrophy (FSHD), which displayed low, yet distinct levels of FRG2 expression, partly from chromosome 4 but predominantly originating from its homolog on chromosome 10. However, in non-FSHD myopathy patients, only distantly related FRG2 homologs were transcribed, whereas differentiating myoblasts from healthy controls failed to express any member of this gene family. In FSHD muscle, genes located upstream of D4Z4 on 4q35, including FRG1, FRG2, and ANT1, are inappropriately overexpressed.

Organism species: Homo sapiens (Human)

CATALOG NO. PRODUCT NAME APPLICATIONS
Proteins n/a Recombinant FSHD Region Gene 2 (FRG2) Recombinant Protein Customized Service Offer
Antibodies n/a Monoclonal Antibody to FSHD Region Gene 2 (FRG2) Monoclonal Antibody Customized Service Offer
n/a Polyclonal Antibody to FSHD Region Gene 2 (FRG2) Polyclonal Antibody Customized Service Offer
Assay Kits n/a CLIA Kit for FSHD Region Gene 2 (FRG2) CLIA Kit Customized Service Offer
n/a ELISA Kit for FSHD Region Gene 2 (FRG2) ELISA Kit Customized Service Offer
  1. "FRG2, an FSHD candidate gene, is transcriptionally upregulated in differentiating primary myoblast cultures of FSHD patients."J. Med. Genet. 41:826-836(2004) [PubMed] [Europe PMC] [Abstract]
  2. "Generation and annotation of the DNA sequences of human chromosomes 2 and 4." Nature 434:724-731(2005) [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]