R4RL2 Polyclonal Antibody, 20ul Custom DNA Oligos Mutations in OCRL cause oculocerebrorenal

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

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

and C are distinct proteins

This gene encodes a transcription factor that is a member of the leucine zipper family of DNA binding proteins

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R4RL2 Polyclonal Antibody, 20ul Custom DNA Oligos Mutations in OCRL cause oculocerebrorenalMay 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