NDUFA3 Polyclonal Antibody, 50ul Transporters A similar but distinct gene

A similar but distinct gene (TAF9L) has been found on the X chromosome and a pseudogene has been identified on chromosome 19

Mutations in this gene are associated with Mitchell-Riley syndrome| which is characterized by neonatal diabetes with pancreatic hypoplasia| duodenal and jejunal atresia| and gall bladder agenesis

These proteins are specifically expressed in the taste receptor cells of the tongue and palate epithelia

which are replaced by Leu residues

Centriolin regulates cell proliferation and contributes to proper entry into the S phase of mitosis

NDUFA3 Polyclonal Antibody, 50ul Transporters A similar but distinct geneNDUFA3 (NADH: ubiquinone Oxidoreductase Subunit A3) 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.