ProfileGDS1065 / 221497_x_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% 83% 81% 80% 81% 75% 78% 69% 79% 67% 68% 68% 79% 84% 82% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1125.874
GSM24653Normal subject 2215.583
GSM24654Normal subject 3250.481
GSM24655A3243G-MELAS subject 111680
GSM24656A3243G-MELAS subject 2188.881
GSM24657A3243G-MELAS subject 3214.475
GSM24658A3243G-MELAS subject 4155.178
GSM24659A3243G-PEO subject 176.869
GSM24660A3243G-PEO subject 2147.779
GSM24661A3243G-PEO subject 361.767
GSM24662A3243G-PEO subject 479.368
GSM24663mtDNA "Common"-deletion subject 196.868
GSM24664mtDNA "Common"-deletion subject 2298.279
GSM24665mtDNA "Common"-deletion subject 3388.384
GSM24666mtDNA "Common"-deletion subject 4353.582