CUL7 Polyclonal Antibody, 100ul Biomatrix Mutations in this gene have

Mutations in this gene have been associated with Pfeiffer syndrome| Jackson-Weiss syndrome|

thyroid hormone and vitamin D3 receptors

Measure MMP-9 levels in human samples and gain valuable insights into potential risks and benefits

Mutations in this gene have been associated with a form of mitochondrial respiratory chain deficiency known as Leigh Syndrome

CELSR3 belongs to the flamingo subfamily

CUL7 Polyclonal Antibody, 100ul Biomatrix Mutations in this gene haveThe protein encoded by this gene is a component of an E3 ubiquitin protein ligase complex. The encoded protein interacts with TP53, CUL9, and FBXW8 proteins. Defects in this gene are a cause of 3M syndrome type 1 (3M1). Two transcript variants encoding different isoforms have been found for this gene.