Op18 Polyclonal Antibody, 100ul[BT-AP06571] Cell Dissociation Mutations in this gene cause

Mutations in this gene cause congenital heart defects| multiple types| 2 (CHTD2)

The protein encoded by this gene is a beta-defensin with antimicrobial activity against E

A pseudogene corresponding to this gene is found on chromosome 1p

Interacts with p53 (TP53)

Family members contain two highly conserved

Op18 Polyclonal Antibody, 100ul[BT-AP06571] Cell Dissociation Mutations in this gene causeSTMN1 belongs to the stathmin family of genes. It encodes a ubiquitous cytosolic phosphoprotein proposed to function as an intracellular relay integrating regulatory signals of the cellular environment. Stathmin 1 is involved in the regulation of the microtubule filament system by destabilizing microtubules. It prevents assembly and promotes disassembly of microtubules. Multiple transcript variants encoding different isoforms have been found for STMN1.