ARHG4 Polyclonal Antibody, 20ul ssDNA Synthesis This protein and ATM share

This protein and ATM share similarity with Schizosaccharomyces pombe rad3

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Mutations in this gene have been shown to cause an X-linked dominant STAR syndrome that typically manifests syndactyly

CSNB1 is a rare inherited retinal disorder characterized by impaired scotopic vision| myopia| hyperopia| nystagmus and reduced visual acuity

ARHG4 Polyclonal Antibody, 20ul ssDNA Synthesis This protein and ATM shareRho GTPases play a fundamental role in numerous cellular processes that are initiated by extracellular stimuli that work through G protein coupled receptors. The protein encoded by this gene may form complex with G proteins and stimulate Rho dependent signals. Multiple alternatively spliced transcript variants encoding different isoforms have been found, but the full length nature of some variants has not been determined.