CUL7 Polyclonal Antibody, 100ul Biomatrix An important paralog of this

An important paralog of this gene is HMP19

whereas beta4GalT enzymes synthesize type 2 carbohydrate chains

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

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

thyroid hormone and vitamin D3 receptors

CUL7 Polyclonal Antibody, 100ul Biomatrix An important paralog of thisThe 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.