ProfileGDS1065 / 210270_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 9% 15% 5% 13% 8% 13% 7% 38% 9% 25% 14% 13% 16% 12% 10% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 13.89
GSM24653Normal subject 25.915
GSM24654Normal subject 32.95
GSM24655A3243G-MELAS subject 14.613
GSM24656A3243G-MELAS subject 24.18
GSM24657A3243G-MELAS subject 36.913
GSM24658A3243G-MELAS subject 42.47
GSM24659A3243G-PEO subject 123.738
GSM24660A3243G-PEO subject 23.99
GSM24661A3243G-PEO subject 38.625
GSM24662A3243G-PEO subject 4514
GSM24663mtDNA "Common"-deletion subject 15.713
GSM24664mtDNA "Common"-deletion subject 212.316
GSM24665mtDNA "Common"-deletion subject 37.212
GSM24666mtDNA "Common"-deletion subject 45.510