ProfileGDS1065 / 204732_s_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 31% 31% 44% 30% 38% 34% 37% 31% 35% 21% 22% 24% 37% 46% 41% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 118.631
GSM24653Normal subject 218.331
GSM24654Normal subject 340.344
GSM24655A3243G-MELAS subject 113.430
GSM24656A3243G-MELAS subject 229.438
GSM24657A3243G-MELAS subject 330.434
GSM24658A3243G-MELAS subject 421.837
GSM24659A3243G-PEO subject 116.631
GSM24660A3243G-PEO subject 221.935
GSM24661A3243G-PEO subject 36.721
GSM24662A3243G-PEO subject 48.622
GSM24663mtDNA "Common"-deletion subject 111.324
GSM24664mtDNA "Common"-deletion subject 24637
GSM24665mtDNA "Common"-deletion subject 355.846
GSM24666mtDNA "Common"-deletion subject 445.241