Dok-1(Phospho Tyr398) Polyclonal Antibody, 100ul Nucleic Acid Amplification Mutations in this gene may

Mutations in this gene may contribute to the congenital central hypoventilation syndrome (CCHS) phenotype in rare cases

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and Cdc16p) domain

this enzyme cleaves alpha 1-proteinase inhibitor but weakly degrades structural proteins of the extracellular matrix

Diseases associated with MAZ include mental retardation

Dok-1(Phospho Tyr398) Polyclonal Antibody, 100ul Nucleic Acid Amplification Mutations in this gene mayThe protein encoded by this gene is part of a signal transduction pathway downstream of receptor tyrosine kinases. The encoded protein is a scaffold protein that helps form a platform for the assembly of multiprotein signaling complexes. Several transcript variants encoding different isoforms have been found for this gene.