CD56 Polyclonal Antibody, 100ul[BT-AP01776] Protein Modification Mutations in this gene cause

Mutations in this gene cause thyroid dyshormonogenesis

Allelic variants of this gene are associated with autosomal dominant mental retardation-32

It is required for N-glycan trimming to Man5-6GlcNAc2 in the endoplasmic-reticulum-associated degradation pathway

encodes a protein that is a member of the small GTPase superfamily

and it moves from the cytoplasm to the cell periphery

CD56 Polyclonal Antibody, 100ul[BT-AP01776] Protein Modification Mutations in this gene causeDDIT3 encodes a member of the CCAAT enhancer binding protein (C EBP) family of transcription factors. DNA damage inducible transcript 3 functions as a dominant negative inhibitor by forming heterodimers with other C EBP members, such as C EBP and LAP (liver activator protein), and preventing their DNA binding activity. The protein is implicated in adipogenesis and erythropoiesis, is activated by endoplasmic reticulum stress, and promotes apoptosis.