CD56 Polyclonal Antibody, 100ul[BT-AP01819] Multi-Layer Cell Culture System Mutations and deletions in NKX2-1

Mutations and deletions in NKX2-1 are associated with benign hereditary chorea

thus functions as a CDK-activating kinase (CAK)

Mutations in this gene can cause X-chromosomal non-specific mental retardation

Similar to its yeast counterpart| this protein is able to interact with the human homolog of yeast Rad6 protein through a conserved ring-finger motif

PR142 (G Protein-Coupled Receptor 142) is a Protein Coding gene

CD56 Polyclonal Antibody, 100ul[BT-AP01819] Multi-Layer Cell Culture System Mutations and deletions in NKX2-1KIT encodes the human homolog of the proto oncogene c kit. C kit was first identified as the cellular homolog of the feline sarcoma viral oncogene v kit. This protein is a type 3 transmembrane receptor for MGF (mast cell growth factor, also known as stem cell factor). Mutations in this gene are associated with gastrointestinal stromal tumors, mast cell disease, acute myelogenous lukemia, and piebaldism. Multiple transcript variants encoding different