MED20 Polyclonal Antibody, 20ul Immune Repertoire Sequencing Mutations in this gene are

Mutations in this gene are associated with megalencep

Donohue syndrome and Rabson-Mendenhall syndrome

mutations in this gene can cause the autosomal recessive form of Robinow syndrome

heart and skeletal muscle

and a tyrosine kinase (TK) domain within the cytoplasmic domain

MED20 Polyclonal Antibody, 20ul Immune Repertoire Sequencing Mutations in this gene areThis gene encodes a component of the mediator complex (also known as TRAP, SMCC, DRIP, or ARC), a transcriptional coactivator complex thought to be required for the expression of almost all genes. The mediator complex is recruited by transcriptional activators or nuclear receptors to induce gene expression, by interacting with RNA polymerase II and promoting the formation of a transcriptional pre initiation complex. A mutation in this gene has been