Gene: PTCD3 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 55037
Gene Symbol: PTCD3
PTCD3 		0.300 Biomarker disease CLINGEN Mitochondrial ribosomal protein PTCD3 mutations cause oxidative phosphorylation defects with Leigh syndrome. 30607703 2019
Entrez Id: 55037
Gene Symbol: PTCD3
PTCD3 		0.300 Biomarker disease CLINGEN Proteomics. Tissue-based map of the human proteome. 25613900 2015
Entrez Id: 55037
Gene Symbol: PTCD3
PTCD3 		0.300 Biomarker disease CLINGEN Pentatricopeptide repeat domain protein 3 associates with the mitochondrial small ribosomal subunit and regulates translation. 19427859 2009