PTCD3 (Pentatricopeptide Repeat Domain 3) is a Protein Coding gene. Diseases associated with PTCD3 include Leigh Syndrome, French Canadian Type and Leigh Syndrome. Among its related pathways are Organelle biogenesis and maintenance and Mitochondrial translation. Gene Ontology (GO) annotations related to this gene include ribosomal small subunit binding.
Immunogen Information
Immunogen
Recombinant fusion protein of human PTCD3 (NP_060422.4).