ProfileGDS1065 / 31826_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 80% 78% 79% 80% 82% 80% 80% 84% 83% 86% 75% 85% 81% 79% 79% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1184.680
GSM24653Normal subject 2150.478
GSM24654Normal subject 3210.679
GSM24655A3243G-MELAS subject 1113.780
GSM24656A3243G-MELAS subject 2205.682
GSM24657A3243G-MELAS subject 3290.580
GSM24658A3243G-MELAS subject 4168.280
GSM24659A3243G-PEO subject 1162.384
GSM24660A3243G-PEO subject 2189.483
GSM24661A3243G-PEO subject 3179.986
GSM24662A3243G-PEO subject 4113.975
GSM24663mtDNA "Common"-deletion subject 1260.285
GSM24664mtDNA "Common"-deletion subject 2346.681
GSM24665mtDNA "Common"-deletion subject 3271.179
GSM24666mtDNA "Common"-deletion subject 4290.479