WNT6 Polyclonal Antibody, 20ul sgRNA Library Construction Mutations in this gene cause

Mutations in this gene cause various glaucoma phenotypes including primary congenital glaucoma

Amplification and/or overexpression of this gene has been reported in numerous cancers| including breast and ovarian tumors

Proteins in this family share a variant EGF-like motif

it couples signals from receptor and cytoplasmic tyrosine kinases to the Ras signaling pathway

WNT6 Polyclonal Antibody, 20ul sgRNA Library Construction Mutations in this gene causeThe WNT gene family consists of structurally related genes which encode secreted signaling proteins. These proteins have been implicated in oncogenesis and in several developmental processes, including regulation of cell fate and patterning during embryogenesis. This gene is a member of the WNT gene family. It is overexpressed in cervical cancer cell line and strongly coexpressed with another family member, WNT10A, in colorectal cancer cell line. The