HRAS Rabbit Monoclonal Antibody

Cell localization:Cytoplasm, Membrane.This gene belongs to the Ras oncogene family, whose members are related to the transforming genes of mammalian sarcoma retroviruses. The products encoded by these genes function in signal transduction pathways. These proteins can bind GTP and GDP, and they have intrinsic GTPase activity. This protein undergoes a continuous cycle of de- and re-palmitoylation, which regμLates its rapid exchange between the plasma membrane and the Golgi apparatus. Mutations in this gene cause Costello syndrome, a disease characterized by increased growth at the prenatal stage, growth deficiency at the postnatal stage, predisposition to tumor formation, cognitive disability, skin and muscμLoskeletal abnormalities, distinctive facial appearance and cardiovascμLar abnormalities. Defects in this gene are implicated in a variety of cancers, including bladder cancer, follicμLar thyroid cancer, and oral squamous cell carcinoma. MμLtiple transcript variants, which encode different isoforms, have been identified for this gene. [provided by RefSeq, JμL 2008]

HRAS, HRAS1, GTPase, H-Ras-1, Ha-Ras, Transforming protein p21, , c-H-ras, p21ras, Cleaved into: GTPase HRas N-terminally processed, Cleaved into: GTPase Hras, GTPase Hras, HRAS 1