ProfileGDS1065 / 204745_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 91% 95% 95% 94% 94% 93% 93% 95% 93% 94% 93% 93% 94% 89% 95% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1499.991
GSM24653Normal subject 2758.695
GSM24654Normal subject 31153.195
GSM24655A3243G-MELAS subject 1459.894
GSM24656A3243G-MELAS subject 2674.294
GSM24657A3243G-MELAS subject 31079.593
GSM24658A3243G-MELAS subject 454393
GSM24659A3243G-PEO subject 1594.795
GSM24660A3243G-PEO subject 2562.793
GSM24661A3243G-PEO subject 3501.794
GSM24662A3243G-PEO subject 4517.493
GSM24663mtDNA "Common"-deletion subject 1692.893
GSM24664mtDNA "Common"-deletion subject 21242.794
GSM24665mtDNA "Common"-deletion subject 3630.289
GSM24666mtDNA "Common"-deletion subject 41660.395