SPG16 Rabbit Polyclonal Antibody, 20ul ROS/Nitric Oxide Detection Diseases associated with NRSN1 include

Diseases associated with NRSN1 include louse-borne relapsing fever

Mutations in DOK7 are a cause of familial limb-girdle myasthenia autosomal recessive

Mutations in this gene are associated with type II Stickler syndrome and with Marshall syndrome

and the acrosome reaction

Studies in mouse suggest that the protein encoded by this gene likely activates basal transcription from class II promoters by interaction with TBP and the class II promoter DNA

SPG16 Rabbit Polyclonal Antibody, 20ul ROS/Nitric Oxide Detection Diseases associated with NRSN1 includeCilia and flagella are comprised of a microtubular backbone the axoneme which is organized by the basal body and surrounded by plasma membrane. SPAG16 encodes 2 major proteins that associate with the axoneme of sperm tail and the nucleus of postmeiotic germ cells respectively (Zhang et al. 2007