CD56 Polyclonal Antibody, 100ul[BT-AP01613] Digital Burette Defects in this gene are

Defects in this gene are a cause of susceptibility to familial hypertrigliceridemia

Among its related pathways are Translation Insulin regulation of translation and Wnt signaling pathway (KEGG)

Spliceosome C Complex Subunit) is a Protein Coding gene

Mutations in this gene are associated with thyroid dyshormonogenesis 1

CD56 Polyclonal Antibody, 100ul[BT-AP01613] Digital Burette Defects in this gene areThe cadherin EGF LAG seven pass G type receptor 2 encoded by CELSR2 is a member of the flamingo subfamily, part of the cadherin superfamily. The flamingo subfamily consists of nonclassic type cadherins; a subpopulation that does not interact with catenins. The flamingo cadherins are located at the plasma membrane and have nine cadherin domains, seven epidermal growth factor like repeats and two laminin A G type repeats in their ectodomain. They also