Nephrocystin-4 Polyclonal Antibody, 20ul Metabolic enzymes Deletions in this gene may

Deletions in this gene may contribute to the etiology of velo-cardio-facial syndrome and DiGeorge syndrome

JAK1 encodes a membrane protein that is a member of a class of protein-tyrosine kinases (PTK) characterized by the presence of a second phosphotransferase-related domain immediately N-terminal to the PTK domain

This protein may play a role as a positive regulator of the Wingless type MMTV integration site signaling pathway

Cyclin D1 encoded by CCND1 belongs to the highly conserved cyclin family

This protein is thought to play a role in multiple cellular processes

Nephrocystin-4 Polyclonal Antibody, 20ul Metabolic enzymes Deletions in this gene mayNPHP4 encodes a protein involved in renal tubular development and function. Nephrocystin 4 interacts with nephrocystin, and belongs to a multifunctional complex that is localized to actin and microtubule based structures. Mutations in this gene are associated with nephronophthisis type 4, a renal disease, and with Senior Loken syndrome type 4, a combination of nephronophthisis and retinitis pigmentosa. Alternative splicing results in multiple