ProfileGDS1065 / 204140_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 62% 68% 57% 66% 62% 62% 65% 60% 45% 62% 59% 54% 60% 55% 63% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 173.462
GSM24653Normal subject 291.268
GSM24654Normal subject 372.857
GSM24655A3243G-MELAS subject 158.766
GSM24656A3243G-MELAS subject 275.462
GSM24657A3243G-MELAS subject 3112.362
GSM24658A3243G-MELAS subject 476.565
GSM24659A3243G-PEO subject 154.660
GSM24660A3243G-PEO subject 233.445
GSM24661A3243G-PEO subject 351.862
GSM24662A3243G-PEO subject 453.159
GSM24663mtDNA "Common"-deletion subject 154.254
GSM24664mtDNA "Common"-deletion subject 2120.260
GSM24665mtDNA "Common"-deletion subject 381.655
GSM24666mtDNA "Common"-deletion subject 4119.263