ProfileGDS1065 / 208651_x_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 33% 44% 33% 22% 9% 35% 40% 26% 26% 39% 33% 10% 4% 32% 28% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 120.833
GSM24653Normal subject 233.344
GSM24654Normal subject 324.333
GSM24655A3243G-MELAS subject 18.322
GSM24656A3243G-MELAS subject 24.69
GSM24657A3243G-MELAS subject 331.735
GSM24658A3243G-MELAS subject 425.340
GSM24659A3243G-PEO subject 112.626
GSM24660A3243G-PEO subject 212.826
GSM24661A3243G-PEO subject 319.239
GSM24662A3243G-PEO subject 418.333
GSM24663mtDNA "Common"-deletion subject 14.210
GSM24664mtDNA "Common"-deletion subject 23.94
GSM24665mtDNA "Common"-deletion subject 328.832
GSM24666mtDNA "Common"-deletion subject 421.828