HIPL1 Rabbit Polyclonal Antibody, 20ul Fluorescent Staining Mutations in this gene are

Mutations in this gene are a cause of X-linked deafness-4| and the encoded protein may play a role in the maintenance of inner ear cells subjected to mechanical stress

The alpha subunit includes the skeletal muscle and hepatic isoforms| and the hepatic isoform is encoded by this gene

tissue specificity:Expressed exclusively in the central nervous system

The encoded protein acts as a repressor when not bound to Notch proteins and an activator when bound to Notch proteins

and AQP6 are closely related and all map to 12q13

HIPL1 Rabbit Polyclonal Antibody, 20ul Fluorescent Staining Mutations in this gene areThis gene encodes a protein that belongs to the glucose sorbosone dehydrogenase family. The encoded protein also contains a domain that binds folate and reduced folic acid derivatives.