ProfileGDS1065 / 209515_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 51% 34% 46% 52% 41% 41% 44% 39% 42% 30% 17% 33% 54% 48% 26% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 145.551
GSM24653Normal subject 221.234
GSM24654Normal subject 343.746
GSM24655A3243G-MELAS subject 134.352
GSM24656A3243G-MELAS subject 232.741
GSM24657A3243G-MELAS subject 342.741
GSM24658A3243G-MELAS subject 43144
GSM24659A3243G-PEO subject 124.339
GSM24660A3243G-PEO subject 229.742
GSM24661A3243G-PEO subject 312.130
GSM24662A3243G-PEO subject 46.217
GSM24663mtDNA "Common"-deletion subject 120.433
GSM24664mtDNA "Common"-deletion subject 292.554
GSM24665mtDNA "Common"-deletion subject 360.148
GSM24666mtDNA "Common"-deletion subject 42026