EI24 Rabbit Polyclonal Antibody, 50ul Molecular Weight Markers Mutations in this gene have

Mutations in this gene have been associated with geleophysic dysplasia

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a putative transmembrane domain

Diseases associated with ZNF608 include renal cell carcinoma

Mutations in this gene cause arginine:glycine amidinotransferase deficiency| an inborn error of creatine synthesis characterized by mental retardation| language impairment| and behavioral disorders

EI24 Rabbit Polyclonal Antibody, 50ul Molecular Weight Markers Mutations in this gene haveThis gene encodes a putative tumor suppressor and has higher expression in p53 expressing cells than in control cells and is an immediate early induction target of p53 mediated apoptosis. The encoded protein may suppress cell growth by inducing apoptotic cell death through the caspase 9 and mitochondrial pathways. This gene is located on human chromosome 11q24 a region frequently altered in cancers. Alternative splicing results in multiple transcript