FGF14 Polyclonal Antibody, 50ul Variant Libraries This gene is a candidate

This gene is a candidate gene for autosomal dominant retinitis pigmentosa

The osteoglycin induces ectopic bone formation in conjunction with transforming growth factor beta and may regulate osteoblast differentiation

The protein encoded by this gene belongs to the gp130 family of cytokine receptors that are known to stimulate gene transcription via activation of cytosolic STAT proteins

This protein localizes to the mitochondrial inner membrane and is involved in the conversion of progesterone to cortisol in the adrenal cortex

Interacts with SERPING1

FGF14 Polyclonal Antibody, 50ul Variant Libraries This gene is a candidateThe protein encoded by this gene is a member of the fibroblast growth factor (FGF) family. FGF family members possess broad mitogenic and cell survival activities, and are involved in a variety of biological processes, including embryonic development, cell growth, morphogenesis, tissue repair, tumor growth and invasion. A mutation in this gene is associated with autosomal dominant cerebral ataxia. Alternatively spliced transcript variants have been