CCDC109A Polyclonal Antibody, 100ul Protein Post-translational Modification Diseases associated with DBX1 include

Diseases associated with DBX1 include Central Hypoventilation Syndrome

biologically inert and non-degradable

a generalized lymphatic dysplasia in humans

Alternative promoter and translation initiation site usage allows this gene to exert spatial and temporal specificity to cAMP responsiveness

The corresponding rat protein has been detected in the pancreas

CCDC109A Polyclonal Antibody, 100ul Protein Post-translational Modification Diseases associated with DBX1 includeMCU (mitochondrial calcium uniporter) encodes a calcium transporter that localizes to the mitochondrial inner membrane. The encoded protein interacts with mitochondrial calcium uptake 1. Alternative splicing results in multiple transcript variants.