ProfileGDS1065 / 207094_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 19% 21% 15% 17% 28% 27% 18% 12% 20% 18% 15% 19% 13% 25% 9% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 18.219
GSM24653Normal subject 29.321
GSM24654Normal subject 3715
GSM24655A3243G-MELAS subject 15.817
GSM24656A3243G-MELAS subject 217.328
GSM24657A3243G-MELAS subject 319.927
GSM24658A3243G-MELAS subject 46.518
GSM24659A3243G-PEO subject 15.212
GSM24660A3243G-PEO subject 28.820
GSM24661A3243G-PEO subject 35.618
GSM24662A3243G-PEO subject 45.515
GSM24663mtDNA "Common"-deletion subject 18.219
GSM24664mtDNA "Common"-deletion subject 29.713
GSM24665mtDNA "Common"-deletion subject 318.825
GSM24666mtDNA "Common"-deletion subject 45.29