PARK2 Polyclonal Antibody, 100ul Custom DNA Oligos Mutations in this gene are

Mutations in this gene are associated with Cenani-Lenz syndrome

F2RL3 is activated by proteolytic cleavage of its extracellular amino terminus

that is found in the basolateral membranes of hepatocytes

GPR37L1 (G Protein-Coupled Receptor 37 Like 1) is a Protein Coding gene

and mediates axon guidance of neuronal growth cones towards sources of netrin 1 ligand

PARK2 Polyclonal Antibody, 100ul Custom DNA Oligos Mutations in this gene areThe precise function of PARK2 is unknown; however, the encoded protein is a component of a multiprotein E3 ubiquitin ligase complex that mediates the targeting of substrate proteins for proteasomal degradation. Mutations in PARK2 are known to cause Parkinson disease and autosomal recessive juvenile Parkinson disease. Alternative splicing of this gene produces multiple transcript variants encoding distinct isoforms. Additional splice variants of this