CD57 Polyclonal Antibody, 50ul[BT-AP01697] Cellular Cultivation & Health Management Mutations in this gene are

Mutations in this gene are the cause of hyperlipoproteinemia| type 1D

These proteins contain luminal carbohydrate recognition domains| which display homology to leguminous lectins

suggesting that these molecules form a complex in trophectoderm cells at the time of implantation

Deregulation of telomerase expression in somatic cells may be involved in oncogenesis

thus may function in signaling pathways utilized broadly during fetal development

CD57 Polyclonal Antibody, 50ul[BT-AP01697] Cellular Cultivation & Health Management Mutations in this gene areCEP41 (centrosomal protein 41) encodes a centrosomal and microtubule binding protein which is predicted to have two coiled coil domains and a rhodanese domain. In human retinal pigment epithelial cells the protein localized to centrioles and cilia. Mutations in CEP41 have been associated with Joubert Syndrome 15; an autosomal recessive ciliopathy and neurological disorder. Alternative splicing results in multiple transcript variants.