ProfileGDS1065 / 222050_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 12% 15% 21% 18% 17% 12% 13% 20% 14% 7% 11% 25% 12% 21% 16% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 15.212
GSM24653Normal subject 26.215
GSM24654Normal subject 310.421
GSM24655A3243G-MELAS subject 16.318
GSM24656A3243G-MELAS subject 2817
GSM24657A3243G-MELAS subject 36.612
GSM24658A3243G-MELAS subject 44.413
GSM24659A3243G-PEO subject 18.620
GSM24660A3243G-PEO subject 2614
GSM24661A3243G-PEO subject 32.47
GSM24662A3243G-PEO subject 43.911
GSM24663mtDNA "Common"-deletion subject 11225
GSM24664mtDNA "Common"-deletion subject 29.112
GSM24665mtDNA "Common"-deletion subject 313.421
GSM24666mtDNA "Common"-deletion subject 49.416