EDA Polyclonal Antibody, 100ul Monoclonal Antibody Preparation This gene encodes a member

This gene encodes a member of the latrophilin subfamily of G-protein coupled receptors (GPCR)

Sulfite oxidase deficiency results in neurological abnormalities which are often fatal at an early age

May determine the distinct specification program of class A neurons in the dorsal part of the spinal cord and suppress specification of class B neurons

The protein encoded by this gene is an inositol 1

Among its related pathways are DNA Double-Strand Break Repair and Fanconi anemia pathway

EDA Polyclonal Antibody, 100ul Monoclonal Antibody Preparation This gene encodes a memberThe protein encoded by EDA (ectodysplasin A) is a type II membrane protein that can be cleaved by furin to produce a secreted form. The encoded protein, which belongs to the tumor necrosis factor family, acts as a homotrimer and may be involved in cell cell signaling during the development of ectodermal organs. Defects in EDA are a cause of ectodermal dysplasia, anhidrotic, which is also known as X linked hypohidrotic ectodermal dysplasia. Several