FSHR Polyclonal Antibody, 50ul[BT-AP03380] Buffer Solutions Mutations in this gene are

Mutations in this gene are associated with an increased risk of atypical hemolytic-uremic syndrome

A non-transcribed pseudogene of GnRHR2 is located on chromosome 14

Polymorphisms in this gene are the basis of the Duffy blood group system

tissue specificity:Expressed in various epithelial cancer cell lines

FSHR Polyclonal Antibody, 50ul[BT-AP03380] Buffer Solutions Mutations in this gene areFollicle stimulating hormone receptor encoded by FSHR belongs to family 1 of G protein coupled receptors. It is the receptor for follicle stimulating hormone and functions in gonad development. Mutations in this gene cause ovarian dysgenesis type 1, and also ovarian hyperstimulation syndrome. Alternative splicing results in multiple transcript variants.