LRWD1 Rabbit Polyclonal Antibody, 100ul Pipette Micro Tips Mutations in this gene are

Mutations in this gene are associated with glycerol kinase deficiency (GKD)

This receptor is probably mediated by the G(s)-class of G-proteins which activate adenylate cyclase (By similarity)

This secreted protein undergoes a complex proteolytic maturation

Ehlers-Danlos syndrome type VIIA

Mutations in this gene cause abnormal migration of neurons during development and disrupt the layering of the cortex| leading to epilepsy| mental retardation| subcortical band heterotopia ("double cortex" syndrome) in females and lissencephaly ("smooth brain&quo

LRWD1 Rabbit Polyclonal Antibody, 100ul Pipette Micro Tips Mutations in this gene areThe protein encoded by this gene interacts with components of the origin recognition complex (ORC) and regulates the formation of the prereplicative complex. The encoded protein stabilizes the ORC and therefore aids in DNA replication. This protein is required for the G1 S phase transition of the cell cycle. In addition the encoded protein binds to trimethylated histone H3 in heterochromatin and recruits the ORC and lysine methyltransferases which