ProfileGDS1065 / 201771_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 92% 89% 91% 88% 90% 88% 90% 90% 91% 92% 91% 92% 87% 90% 88% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1529.992
GSM24653Normal subject 234389
GSM24654Normal subject 3570.591
GSM24655A3243G-MELAS subject 119788
GSM24656A3243G-MELAS subject 2401.790
GSM24657A3243G-MELAS subject 3565.388
GSM24658A3243G-MELAS subject 4373.290
GSM24659A3243G-PEO subject 127790
GSM24660A3243G-PEO subject 2424.491
GSM24661A3243G-PEO subject 3331.392
GSM24662A3243G-PEO subject 437491
GSM24663mtDNA "Common"-deletion subject 1521.392
GSM24664mtDNA "Common"-deletion subject 2541.487
GSM24665mtDNA "Common"-deletion subject 365990
GSM24666mtDNA "Common"-deletion subject 4575.888