Wnt-10b Monoclonal Antibody, 50ul Immune Repertoire Sequencing Mutations in KAL1 cause the

Mutations in KAL1 cause the X-linked Kallmann syndrome

and may be involved in early development of the heart

The two variants are differentially expressed in embryonic tissues

at least one of which encodes an isoform that undergoes proteolytic processing

Wnt-10b Monoclonal Antibody, 50ul Immune Repertoire Sequencing Mutations in KAL1 cause theThe WNT gene family consists of structurally related genes which encode secreted signaling proteins. These proteins have been implicated in oncogenesis and in several developmental processes, including regulation of cell fate and patterning during embryogenesis. This gene is a member of the WNT gene family. It may be involved in breast cancer, and its protein signaling is likely a molecular switch that governs adipogenesis. This protein is 96%