ProfileGDS1065 / 212103_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 87% 81% 82% 82% 81% 79% 80% 79% 82% 83% 83% 86% 80% 84% 82% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1307.687
GSM24653Normal subject 2187.781
GSM24654Normal subject 3268.782
GSM24655A3243G-MELAS subject 1125.282
GSM24656A3243G-MELAS subject 2192.881
GSM24657A3243G-MELAS subject 327579
GSM24658A3243G-MELAS subject 4174.580
GSM24659A3243G-PEO subject 1125.279
GSM24660A3243G-PEO subject 2181.182
GSM24661A3243G-PEO subject 3154.583
GSM24662A3243G-PEO subject 4175.583
GSM24663mtDNA "Common"-deletion subject 1287.686
GSM24664mtDNA "Common"-deletion subject 2326.280
GSM24665mtDNA "Common"-deletion subject 3382.484
GSM24666mtDNA "Common"-deletion subject 4358.382