ProfileGDS1065 / 208619_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 94% 93% 93% 94% 93% 92% 94% 93% 94% 93% 94% 94% 95% 93% 93% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1794.394
GSM24653Normal subject 2537.893
GSM24654Normal subject 3822.193
GSM24655A3243G-MELAS subject 1410.594
GSM24656A3243G-MELAS subject 2601.393
GSM24657A3243G-MELAS subject 3919.792
GSM24658A3243G-MELAS subject 4730.994
GSM24659A3243G-PEO subject 1409.993
GSM24660A3243G-PEO subject 2599.594
GSM24661A3243G-PEO subject 3407.593
GSM24662A3243G-PEO subject 4551.994
GSM24663mtDNA "Common"-deletion subject 169994
GSM24664mtDNA "Common"-deletion subject 21445.495
GSM24665mtDNA "Common"-deletion subject 31034.393
GSM24666mtDNA "Common"-deletion subject 41179.393