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

Mutations in this gene cause thyroid dyshormonogenesis

This gene belongs to a family of alpha-amino-3-hydroxy-5-methyl-4-isoxazole propionate (AMPA) receptors

and a carboxy-terminal regulatory domain that mediates homodimerization

|subunit:Interacts with DYSF

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.