ProfileGDS1065 / 201751_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 57% 56% 65% 40% 50% 61% 61% 41% 54% 66% 31% 56% 64% 67% 65% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 159.857
GSM24653Normal subject 254.856
GSM24654Normal subject 3101.465
GSM24655A3243G-MELAS subject 122.440
GSM24656A3243G-MELAS subject 24850
GSM24657A3243G-MELAS subject 3107.361
GSM24658A3243G-MELAS subject 464.461
GSM24659A3243G-PEO subject 12741
GSM24660A3243G-PEO subject 248.654
GSM24661A3243G-PEO subject 360.966
GSM24662A3243G-PEO subject 415.931
GSM24663mtDNA "Common"-deletion subject 158.956
GSM24664mtDNA "Common"-deletion subject 2143.364
GSM24665mtDNA "Common"-deletion subject 3138.167
GSM24666mtDNA "Common"-deletion subject 4135.965