WB, ELISA, ICC/IF, IPHost:
Applications: WB, ICC/IF
Host: Mouse Polyclonal
Applications: WB, ELISA, PA, PAGE, AP
Applications: WB, ELISA, PA, AP
FRG1 maps to a location 100 kb centromeric of the repeat units on chromosome 4q35 which are deleted in facioscapulohumeral muscular dystrophy (FSHD). It is evolutionarily conserved and has related sequences on multiple human chromosomes but DNA sequence analysis did not reveal any homology to known genes. In vivo studies demonstrate the encoded protein is localized to the nucleolus.
|Product By Gene ID
- protein FRG1
- facioscapulohumeral muscular dystrophy region gene-1
- FSHD region gene 1 protein
- FSHD region gene 1
Bioinformatics Tool for FRG1
Discover related pathways, diseases and genes to FRG1. Need help? Read the Bioinformatics Tool Guide
for instructions on using this tool.