ProfileGDS1065 / 205074_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 78% 86% 76% 78% 80% 79% 72% 78% 70% 81% 79% 79% 78% 77% 74% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1160.178
GSM24653Normal subject 2257.386
GSM24654Normal subject 3181.976
GSM24655A3243G-MELAS subject 1100.478
GSM24656A3243G-MELAS subject 2179.880
GSM24657A3243G-MELAS subject 3262.879
GSM24658A3243G-MELAS subject 4108.572
GSM24659A3243G-PEO subject 1113.478
GSM24660A3243G-PEO subject 290.870
GSM24661A3243G-PEO subject 3134.481
GSM24662A3243G-PEO subject 4138.379
GSM24663mtDNA "Common"-deletion subject 1180.979
GSM24664mtDNA "Common"-deletion subject 2281.378
GSM24665mtDNA "Common"-deletion subject 3234.877
GSM24666mtDNA "Common"-deletion subject 4213.974