ProfileGDS1065 / 221498_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 79% 80% 80% 74% 82% 73% 76% 77% 77% 75% 80% 75% 80% 75% 77% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1170.679
GSM24653Normal subject 2170.180
GSM24654Normal subject 323680
GSM24655A3243G-MELAS subject 182.174
GSM24656A3243G-MELAS subject 2197.182
GSM24657A3243G-MELAS subject 3192.573
GSM24658A3243G-MELAS subject 4135.876
GSM24659A3243G-PEO subject 1112.277
GSM24660A3243G-PEO subject 2129.377
GSM24661A3243G-PEO subject 391.775
GSM24662A3243G-PEO subject 4149.280
GSM24663mtDNA "Common"-deletion subject 1136.275
GSM24664mtDNA "Common"-deletion subject 2327.680
GSM24665mtDNA "Common"-deletion subject 3203.375
GSM24666mtDNA "Common"-deletion subject 426277