PCDA9 Rabbit Polyclonal Antibody, 20ul Insect Expression Mutations in this gene are

Mutations in this gene are associated with Leigh syndrome resulting from mitochondrial complex I deficiency

GO annotations related to this gene include hydrolase activity and palmitoyl-CoA hydrolase activity

Mutations in this gene have been associated with autosomal recessive megalencephaly

This gene encodes a member of the ubiquitin-specific processing (UBP) family of proteases and is a deubiquitinating enzyme (DUB) with His and Cys domains

where one CBLB peptide binds two copies of the other protein

PCDA9 Rabbit Polyclonal Antibody, 20ul Insect Expression Mutations in this gene areThis gene is a member of the protocadherin alpha gene cluster one of three related gene clusters tandemly linked on chromosome five that demonstrate an unusual genomic organization similar to that of B cell and T cell receptor gene clusters. The alpha gene cluster is composed of 15 cadherin superfamily genes related to the mouse CNR genes and consists of 13 highly similar and 2 more distantly related coding sequences. The tandem array of 15 N terminal