IIGP5 Polyclonal Antibody, 100ul Cell Screening and Imaging Multiple alternatively spliced transcript variants

Multiple alternatively spliced transcript variants of this gene encoding distinct isoforms have been reported

Evidence indicates that mutations in this gene are responsible for the primary defects in patients with progressive myoclonic epilepsy (EPM1)

TBX22 is a member of a phylogenetically conserved family of genes that share a common DNA-binding domain

a familial cardiac and skeletal myopathy (CSM)

This protein has been shown to play a role in homologous recombination related repair of DNA double-strand breaks

IIGP5 Polyclonal Antibody, 100ul Cell Screening and Imaging Multiple alternatively spliced transcript variantsCatalytic activity: GTP + H(2)O = GDP + phosphate. Belongs to the interferon inducible GTPase family.