NDUFC2 Polyclonal Antibody, 20ul ADME Mutations in this gene cause

Mutations in this gene cause nemaline myopathy type 3

Adenosine monophosphate deaminase 1 catalyzes the deamination of AMP to IMP in skeletal muscle and plays an important role in the purine nucleotide cycle

Six alternatively spliced transcript variants encoding different isoforms have been reported

It has higher identity to E2F4 than to other family members

It plays a role in the development of the eyes

NDUFC2 Polyclonal Antibody, 20ul ADME Mutations in this gene causeNDUFC2 (NADH: ubiquinone Oxidoreductase Subunit C2) is a Protein Coding gene. Among its related pathways are Alzheimer's disease and Respiratory electron transport, ATP synthesis by chemiosmotic coupling, and heat production by uncoupling proteins. GO annotations related to this gene include NADH dehydrogenase (ubiquinone) activity. An important paralog of this gene is NDUFC2 KCTD14.