Septin 2 Polyclonal Antibody, 20ul Modified Oligos Mutations in this gene have

Mutations in this gene have been found in ectodermal dysplasia anhidrotic with T-cell immunodeficiency autosomal dominant disease

This cyclin has been shown to specifically interact with CIP/KIP family of CDK inhibitors

which is important for the formation of the skin barrier

HOXB4 is a member of the Antp homeobox family and encodes a nuclear protein with a homeobox DNA-binding domain

Septin 2 Polyclonal Antibody, 20ul Modified Oligos Mutations in this gene haveSEPT2 (Septin 2) is a Protein Coding gene. Diseases associated with SEPT2 include gastrointestinal anthrax and acute orbital inflammation. Among its related pathways are Bacterial invasion of epithelial cells and ERK Signaling. GO annotations related to this gene include GTP binding and enzyme regulator activity. An important paralog of this gene is SEPT6.