ADAT3 Rabbit Polyclonal Antibody, 20ul Centrifuges Muatations in this gene cause

Muatations in this gene cause pseudohypoaldosteronism type IID (PHA2D)

cell metabolism

The protein encoded by this gene is a GTPase activator| working with the GTPase CDC42 to negatively regulate neuronal migration

is not inhibited by warfarin

ADAT3 Rabbit Polyclonal Antibody, 20ul Centrifuges Muatations in this gene causeThis gene encodes a subunit of a tRNA specific adenosine deaminase. This heterodimeric enzyme converts adenosine to inosine in the tRNA anticodon. A mutation in this gene causes a syndrome characterized by intellectual disability and strabismus. This gene shares its 5' exon with the overlapping gene, secretory carrier membrane protein 4 (Gene ID: 113178).