IKK Gamma Polyclonal Antibody, 50ul[BT-AP04426] Site-directed Mutagenesis Mutations in this gene cause

Mutations in this gene cause platelet glycoprotein deficiency

This protein forms a very tight complex with alpha neurexins

This gene encodes a member of the synaptotagmin protein family

Mutations in this gene have been reported to be associated with nonsyndromic hearing loss

These products include the cardiac natriuretic peptides CNP-53

IKK Gamma Polyclonal Antibody, 50ul[BT-AP04426] Site-directed Mutagenesis Mutations in this gene causeIKBKG encodes the regulatory subunit of the inhibitor of kappaB kinase (IKK) complex, which activates NF kappaB resulting in activation of genes involved in inflammation, immunity, cell survival, and other pathways. Mutations in this gene result in incontinentia pigmenti, hypohidrotic ectodermal dysplasia, and several other types of immunodeficiencies. A pseudogene highly similar to this locus is located in an adjacent region of the X chromosome.