ProfileGDS1065 / 202339_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% 50% 52% 48% 35% 61% 50% 46% 54% 42% 59% 35% 40% 48% 49% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 154.355
GSM24653Normal subject 243.250
GSM24654Normal subject 357.152
GSM24655A3243G-MELAS subject 129.848
GSM24656A3243G-MELAS subject 225.535
GSM24657A3243G-MELAS subject 3104.661
GSM24658A3243G-MELAS subject 439.150
GSM24659A3243G-PEO subject 132.846
GSM24660A3243G-PEO subject 248.754
GSM24661A3243G-PEO subject 322.642
GSM24662A3243G-PEO subject 454.359
GSM24663mtDNA "Common"-deletion subject 122.735
GSM24664mtDNA "Common"-deletion subject 251.940
GSM24665mtDNA "Common"-deletion subject 360.648
GSM24666mtDNA "Common"-deletion subject 462.349