ProfileGDS1065 / 220060_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 17% 25% 16% 17% 28% 26% 14% 28% 23% 27% 17% 30% 20% 19% 24% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 17.517
GSM24653Normal subject 212.125
GSM24654Normal subject 37.716
GSM24655A3243G-MELAS subject 15.817
GSM24656A3243G-MELAS subject 216.728
GSM24657A3243G-MELAS subject 319.126
GSM24658A3243G-MELAS subject 44.714
GSM24659A3243G-PEO subject 114.528
GSM24660A3243G-PEO subject 210.523
GSM24661A3243G-PEO subject 31027
GSM24662A3243G-PEO subject 46.417
GSM24663mtDNA "Common"-deletion subject 117.130
GSM24664mtDNA "Common"-deletion subject 216.420
GSM24665mtDNA "Common"-deletion subject 311.619
GSM24666mtDNA "Common"-deletion subject 416.924