Neurexin IIIBeta Polyclonal Antibody, 50ul Peptide Modification Mutations in this gene are

Mutations in this gene are associated with the autosomal recessive disorders cystic fibrosis and congenital bilateral aplasia of the vas deferens

also known as the tetraspanin family

cause neurodegenerative diseases commonly known as Batten disease or collectively known as neuronal ceroid lipofuscinoses (NCLs)

A highly similar protein in mouse has both ferrireductase and cupric reductase activity

Neurexin IIIBeta Polyclonal Antibody, 50ul Peptide Modification Mutations in this gene areNRXN3 (neurexin 3) encodes a member of a family of proteins that function in the nervous system as receptors and cell adhesion molecules. Extensive alternative splicing and the use of alternative promoters results in multiple transcript variants and protein isoforms for this gene, but the full length nature of many of these variants has not been determined. Transcripts that initiate from an upstream promoter encode alpha isoforms, which contain