ProfileGDS1065 / 211599_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 55% 52% 74% 74% 67% 62% 64% 62% 71% 59% 63% 68% 63% 65% 58% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 155.355
GSM24653Normal subject 246.652
GSM24654Normal subject 3161.574
GSM24655A3243G-MELAS subject 182.174
GSM24656A3243G-MELAS subject 29367
GSM24657A3243G-MELAS subject 3112.562
GSM24658A3243G-MELAS subject 472.764
GSM24659A3243G-PEO subject 158.462
GSM24660A3243G-PEO subject 297.271
GSM24661A3243G-PEO subject 345.359
GSM24662A3243G-PEO subject 463.363
GSM24663mtDNA "Common"-deletion subject 1100.868
GSM24664mtDNA "Common"-deletion subject 2136.663
GSM24665mtDNA "Common"-deletion subject 3124.765
GSM24666mtDNA "Common"-deletion subject 496.358