UBPH Polyclonal Antibody, 100ul Protein Analysis Defects in this gene are

Defects in this gene are a cause of macular corneal dystrophy (MCD)

This protein is deleted in some patients with Wilms tumor-Aniridia-Genitourinary anomalies-mental Retardation (WAGR) syndrome

The protein encoded by this gene regulates G protein-coupled receptor phosphorylation in a calcium-dependent manner and can substitute for calmodulin

Members of this family act as an integration point for multiple biochemical signals and are involved in a wide variety of cellular processes such as proliferation| differentiation| transcription regulation| and development

UBPH Polyclonal Antibody, 100ul Protein Analysis Defects in this gene areUBFD1 (Ubiquitin Family Domain Containing 1) is a Protein Coding gene. GO annotations related to this gene include poly (A) RNA binding.