IIGP5 Polyclonal Antibody, 100ul Cell Screening and Imaging TBX22 is a member of

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

Wiskott-Aldrich syndrome is a rare

Gene Ontology (GO) annotations related to this gene include poly(A) RNA binding and N-acetyltransferase activity

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

Interleukin 17A and its receptor play a pathogenic role in many inflammatory and autoimmune diseases such as rheumatoid arthritis

IIGP5 Polyclonal Antibody, 100ul Cell Screening and Imaging TBX22 is a member ofCatalytic activity: GTP + H(2)O = GDP + phosphate. Belongs to the interferon inducible GTPase family.