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

and it moves from the cytoplasm to the cell periphery

It is a member of the p160/steroid receptor coactivator (SRC) family and like other family members has histone acetyltransferase activity and contains a nuclear localization signal

This gene is adjacent to another family member CLDN9 on chromosome 16

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.