MYOC Polyclonal Antibody, 20ul Immunology Mutations in PARK2 are known

Mutations in PARK2 are known to cause Parkinson disease and autosomal recessive juvenile Parkinson disease

subunit:Interacts with FGF1

This locus encodes both the light and heavy subunits of acyloxyacyl hydrolase

suggesting a role as a tumor suppressor gene

a disorder characterized by urinary salt wasting

MYOC Polyclonal Antibody, 20ul Immunology Mutations in PARK2 are knownMYOC encodes the protein myocilin, which is believed to have a role in cytoskeletal function. MYOC is expressed in many occular tissues, including the trabecular meshwork, and was revealed to be the trabecular meshwork glucocorticoid inducible response protein (TIGR). The trabecular meshwork is a specialized eye tissue essential in regulating intraocular pressure, and mutations in MYOC have been identified as the cause of hereditary juvenile onset