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RHG20 Polyclonal Antibody, 100ul Modification Enzymes Mutations in this gene are

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RHG20 Polyclonal Antibody, 100ul Modification Enzymes Mutations in this gene areThe protein encoded by this gene is an activator of RHO type GTPases, transducing a signal from RAP1 to RHO and impacting neurite outgrowth.

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Description

Mutations in this gene are associated with all forms of dystrophic epidermolysis bullosa

The primary function of the encoded transmembrane protein is the induction of apoptosis triggered by binding to FAS

The protein binds both insulin-like growth factors (IGFs) I and II and circulates in the plasma in both glycosylated and non-glycosylated forms

Defects in this gene are a cause of Peters-plus syndrome (PPS)

Transcripts originating from an upstream promoter and capable of expressing a protein with a longer N-terminus have been found

RHG20 Polyclonal Antibody, 100ul Modification Enzymes Mutations in this gene areThe protein encoded by this gene is an activator of RHO type GTPases, transducing a signal from RAP1 to RHO and impacting neurite outgrowth.

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