SYNJ2 Rabbit Polyclonal Antibody, 20ul Human Genome Knockout Libraries In mouse| deletion of this

In mouse| deletion of this homologous gene causes congenital heart disorder known as noncompaction of left ventricular myocardium

Vimentin encoded by this gene is responsible for maintaining cell shape

Essential role in the control of RELA transcriptional activity in response to TNF

Alternatively spliced transcript variants of this gene have been reported

HAAO catalyzes the synthesis of quinolinic acid (QUIN) from 3-hydroxyanthranilic acid

SYNJ2 Rabbit Polyclonal Antibody, 20ul Human Genome Knockout Libraries In mouse| deletion of thisThe gene is a member of the inositol polyphosphate 5 phosphatase family. The encoded protein interacts with the ras related C3 botulinum toxin substrate 1 which causes translocation of the encoded protein to the plasma membrane where it inhibits clathrin mediated endocytosis. Alternative splicing results in multiple transcript variants.