AMMR1 Rabbit Polyclonal Antibody, 50ul Diagnostic Probes & Oligos Diseases associated with SEPT2 include

Diseases associated with SEPT2 include gastrointestinal anthrax and acute orbital inflammation

conserved DNA elements (heat shock elements or HSEs) and CCAAT boxes

This dissociation from the centrosome is phosphorylation-dependent

The enzyme encoded by this gene is active on phenols

AMMR1 Rabbit Polyclonal Antibody, 50ul Diagnostic Probes & Oligos Diseases associated with SEPT2 includeThe exact function of this gene is not known, however, submicroscopic deletion of the X chromosome including this gene, COL4A5, and FACL4 genes, result in a contiguous gene deletion syndrome, the AMME complex (Alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis). Alternatively spliced transcript variants encoding different isoforms have been found for this gene.