EBP1 Polyclonal Antibody, 50ul Cell Biology Mutations in this gene are

Mutations in this gene are the cause of Wagner syndrome type 1

The protein encoded by this gene is highly similar to the gene product of Schizosaccharomyces pombe rad17

Another locus encoding a bipartite transcript designated POMZP3 contains a duplication of the last four exons of ZP3| including the above described variation| and maps closely to this gene

Slit proteins play highly conserved roles in axon guidance and neuronal migration and may also have functions during other cell migration processes including leukocyte migration

Autoantibodies against the encoded protein have been detected in serum from patients with type 1 diabetes

EBP1 Polyclonal Antibody, 50ul Cell Biology Mutations in this gene areThis gene encodes an RNA binding protein that is involved in growth regulation. This protein is present in pre ribosomal ribonucleoprotein complexes and may be involved in ribosome assembly and the regulation of intermediate and late steps of rRNA processing. This protein can interact with the cytoplasmic domain of the ErbB3 receptor and may contribute to transducing growth regulatory signals. This protein is also a transcriptional co repressor of