CNDD3 Polyclonal Antibody, 50ul Bottles Variations in this gene may

Variations in this gene may increase the risk of prostate cancer

similarity:Contains 1 basic helix-loop-helix (bHLH) domain

The gene consists of 12 exons and the genomic structure is similar to that of neuregulin 1

UPF1 (UPF1

Mutations in this gene cause Gitelman syndrome| a disease similar to Bartter's syndrome| that is characterized by hypokalemic alkalosis combined with hypomagnesemia| low urinary calcium| and increased renin activity associated with normal blood pressure

CNDD3 Polyclonal Antibody, 50ul Bottles Variations in this gene mayCondensin complexes I and II play essential roles in mitotic chromosome assembly and segregation. Both condensins contain 2 invariant structural maintenance of chromosome (SMC) subunits, SMC2 (MIM 605576) and SMC4 (MIM 605575), but they contain different sets of non SMC subunits. NCAPD3 is 1 of 3 non SMC subunits that define condensin II (Ono et al., 2003