FoxC1/2 Polyclonal Antibody, 20ul Pipette Micro Tips Mutations in CACNA2D1 can cause

Mutations in CACNA2D1 can cause cardiac deficiencies

Cut like homeobox 1 encoded by CUX1 is a member of the homeodomain family of DNA binding proteins

The Ab hydrolase domain containing (ABHD) gene subfamily is comprised of 15 mostly uncharacterized members

Proteins containing arm repeats are involved in development

Cdc7-Dbf4 efficiently phosphorylates several proteins that are required for the initiation of DNA replication

FoxC1/2 Polyclonal Antibody, 20ul Pipette Micro Tips Mutations in CACNA2D1 can causeFOXC1 belongs to the forkhead family of transcription factors which is characterized by a distinct DNA binding forkhead domain. The specific function of this gene has not yet been determined; however, it has been shown to play a role in the regulation of embryonic and ocular development. Mutations in this gene cause various glaucoma phenotypes including primary congenital glaucoma, autosomal dominant iridogoniodysgenesis anomaly, and Axenfeld Rieger