CXL14 Polyclonal Antibody, 100ul Culture Tubes Mutations in this gene have

Mutations in this gene have been associated with the X-linked form of Opitz syndrome

It is one of seven related genes or pseudogenes found in a cluster| thought to result from gene duplication| on chromosome 22

where it is differentially expressed during differentiation

|tissue specificity:Leukemic stem cell

Mutations in this gene cause juvenile myoclonic epilepsy and childhood absence epilepsy type 4

CXL14 Polyclonal Antibody, 100ul Culture Tubes Mutations in this gene haveThis antimicrobial gene belongs to the cytokine gene family which encode secreted proteins involved in immunoregulatory and inflammatory processes. The protein encoded by this gene is structurally related to the CXC (Cys X Cys) subfamily of cytokines. Members of this subfamily are characterized by two cysteines separated by a single amino acid. This cytokine displays chemotactic activity for monocytes but not for lymphocytes, dendritic cells,