ProfileGDS1065 / 210952_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 20% 9% 36% 21% 21% 33% 40% 43% 51% 21% 29% 14% 33% 16% 31% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1920
GSM24653Normal subject 249
GSM24654Normal subject 327.536
GSM24655A3243G-MELAS subject 17.721
GSM24656A3243G-MELAS subject 210.821
GSM24657A3243G-MELAS subject 329.133
GSM24658A3243G-MELAS subject 425.940
GSM24659A3243G-PEO subject 128.543
GSM24660A3243G-PEO subject 242.951
GSM24661A3243G-PEO subject 3721
GSM24662A3243G-PEO subject 41429
GSM24663mtDNA "Common"-deletion subject 16.114
GSM24664mtDNA "Common"-deletion subject 237.833
GSM24665mtDNA "Common"-deletion subject 39.516
GSM24666mtDNA "Common"-deletion subject 426.631