ProfileGDS1065 / 210330_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 53% 38% 48% 51% 46% 45% 46% 58% 39% 56% 42% 38% 34% 44% 44% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 150.653
GSM24653Normal subject 225.538
GSM24654Normal subject 347.548
GSM24655A3243G-MELAS subject 133.651
GSM24656A3243G-MELAS subject 240.346
GSM24657A3243G-MELAS subject 350.645
GSM24658A3243G-MELAS subject 433.846
GSM24659A3243G-PEO subject 149.658
GSM24660A3243G-PEO subject 225.939
GSM24661A3243G-PEO subject 339.856
GSM24662A3243G-PEO subject 427.542
GSM24663mtDNA "Common"-deletion subject 126.938
GSM24664mtDNA "Common"-deletion subject 240.534
GSM24665mtDNA "Common"-deletion subject 351.444
GSM24666mtDNA "Common"-deletion subject 451.644