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

Muatations in this gene cause pseudohypoaldosteronism type IID (PHA2D)

is not inhibited by warfarin

Mutations in this gene are associated with platelet-type bleeding disorders

cell metabolism

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

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).