Source: ALL

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 107075310
Gene Symbol: MTCO2P12
MTCO2P12
CUI: C0162671
Disease: MELAS Syndrome
MELAS Syndrome 		0.020 GeneticVariation BEFREE High prevalence of the COII/tRNA(Lys) intergenic 9-bp deletion in mitochondrial DNA of Taiwanese patients with MELAS or MERRF syndrome. 15965049

2005
Entrez Id: 107075310
Gene Symbol: MTCO2P12
MTCO2P12
CUI: C0162671
Disease: MELAS Syndrome
MELAS Syndrome 		0.020 Biomarker BEFREE The pattern of expression of genes for mtDNA-encoded ribosomal RNA and the protein-coding region cytochrome c oxidase subunit II were similar in muscle specimens of patients with MELAS, patients with chronic progressive external ophthalmoplegia, and normal control subjects, and also between the two MELAS mutations. 7684581

1993