Fer Polyclonal Antibody, 50ul[BT-AP03193] sgRNA Oligos Defects in this gene are

Defects in this gene are the cause of Werner syndrome| an autosomal recessive disorder characterized by premature aging

The encoded peroxisomal protein utilizes saturated fatty acids of 16 or 18 carbons as preferred substrates

EIF3G and EIF3I

and renal and muscular defects

Fer Polyclonal Antibody, 50ul[BT-AP03193] sgRNA Oligos Defects in this gene areTyrosine protein kinase Fer encoded by FER is a member of the FPS FES family of non transmembrane receptor tyrosine kinases. It regulates cell cell adhesion and mediates signaling from the cell surface to the cytoskeleton via growth factor receptors. Alternative splicing results in multiple transcript variants. A related pseudogene has been identified on chromosome X.