ProfileGDS1065 / 215860_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 21% 32% 25% 25% 16% 27% 31% 31% 48% 37% 40% 25% 19% 13% 29% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 19.421
GSM24653Normal subject 219.432
GSM24654Normal subject 31425
GSM24655A3243G-MELAS subject 19.925
GSM24656A3243G-MELAS subject 27.616
GSM24657A3243G-MELAS subject 32027
GSM24658A3243G-MELAS subject 41631
GSM24659A3243G-PEO subject 116.731
GSM24660A3243G-PEO subject 237.848
GSM24661A3243G-PEO subject 317.937
GSM24662A3243G-PEO subject 425.440
GSM24663mtDNA "Common"-deletion subject 112.625
GSM24664mtDNA "Common"-deletion subject 215.519
GSM24665mtDNA "Common"-deletion subject 37.413
GSM24666mtDNA "Common"-deletion subject 423.629