ProfileGDS1065 / 205530_at
TitleMitochondrial encephalomyopathies associated with mitochondrial DNA mutations
OrganismHomo sapiens


wild type A3243G large deletion normal MELAS PEO GSM24652 GSM24653 GSM24654 GSM24655 GSM24656 GSM24657 GSM24658 GSM24659 GSM24660 GSM24661 GSM24662 GSM24663 GSM24664 GSM24665 GSM24666 74% 84% 79% 87% 84% 79% 78% 78% 77% 75% 78% 78% 83% 78% 84% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1132.274
GSM24653Normal subject 2217.584
GSM24654Normal subject 3213.179
GSM24655A3243G-MELAS subject 1182.687
GSM24656A3243G-MELAS subject 2240.184
GSM24657A3243G-MELAS subject 3276.179
GSM24658A3243G-MELAS subject 415378
GSM24659A3243G-PEO subject 1118.478
GSM24660A3243G-PEO subject 2128.877
GSM24661A3243G-PEO subject 389.675
GSM24662A3243G-PEO subject 4130.178
GSM24663mtDNA "Common"-deletion subject 1171.378
GSM24664mtDNA "Common"-deletion subject 2399.883
GSM24665mtDNA "Common"-deletion subject 3244.378
GSM24666mtDNA "Common"-deletion subject 4411.984