ProfileGDS1065 / 211001_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 49% 51% 50% 52% 49% 47% 46% 48% 56% 50% 49% 53% 55% 50% 38% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 143.249
GSM24653Normal subject 244.451
GSM24654Normal subject 352.450
GSM24655A3243G-MELAS subject 135.152
GSM24656A3243G-MELAS subject 245.449
GSM24657A3243G-MELAS subject 356.847
GSM24658A3243G-MELAS subject 432.646
GSM24659A3243G-PEO subject 134.848
GSM24660A3243G-PEO subject 251.956
GSM24661A3243G-PEO subject 331.150
GSM24662A3243G-PEO subject 435.949
GSM24663mtDNA "Common"-deletion subject 152.353
GSM24664mtDNA "Common"-deletion subject 297.455
GSM24665mtDNA "Common"-deletion subject 363.850
GSM24666mtDNA "Common"-deletion subject 439.338