R4RL2 Polyclonal Antibody, 20ul Custom DNA Oligos Polymorphisms in this gene have

Polymorphisms in this gene have been linked to various human diseases| including IgA deficiency| common variable immunodeficiency| and premature ovarian failure

RhoGEF kinase) encodes a protein that interacts with the huntingtin-associated protein 1

Mutations in OCRL cause oculocerebrorenal syndrome of Lowe and also Dent disease

including the C5 alpha chain

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R4RL2 Polyclonal Antibody, 20ul Custom DNA Oligos Polymorphisms in this gene haveMay play a role in regulating axonal regeneration and plasticity in the adult central nervous system.,PTM: Undergoes zinc metalloproteinase mediated ectodomain shedding in neuroblastoma cells; where BRE is released as a full length ectodomain and an N terminal fragment containing the leucine rich repeat (LRR) region of the protein.,Belongs to the Nogo receptor family.,Contains 8 LRR (leucine rich) repeats.,subcellular location: Localized to the