NCIt definition : Human NODAL wild-type allele is located in the vicinity of 10q22.1 and is approximately
10 kb in length. This allele, which encodes nodal homolog protein, plays a role in
the modulation of embryonic mesoderm and axis formation. Mutation of the gene is associated
with visceral heterotaxy autosomal type 5.;
NCIt note : The NODAL gene and the ACVR1C gene may suppress ovarian cancer cell proliferation.
(J. Clin. Endocrinol. Metab. 2004; 89: 5523-5534.);