CPXCR Polyclonal Antibody, 100ul Hybridoma Antibody Sequencing An important paralog of this

An important paralog of this gene is SNRK

thus reducing contamination of the medium or evaporation loss during the cell culture process

Disruption of this gene is associated with focal epilepsy and speech disorder with or without mental retardation

AMIGO family

CPXCR Polyclonal Antibody, 100ul Hybridoma Antibody Sequencing An important paralog of thisThis gene is one of several genes identified in a region of the X chromosome associated with an X linked cleft palate (CPX) disorder. The encoded protein contains a motif similar to a motif found in zinc finger proteins. Mutation analysis of this gene has not revealed any mutation which causes the CPX disorder. Multiple alternatively spliced variants, encoding the same protein, have been identified.