ProfileGDS1065 / 208641_s_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 95% 95% 93% 94% 93% 95% 93% 95% 93% 96% 95% 95% 95% 93% 95% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1925.895
GSM24653Normal subject 2829.395
GSM24654Normal subject 3747.593
GSM24655A3243G-MELAS subject 1388.594
GSM24656A3243G-MELAS subject 2572.993
GSM24657A3243G-MELAS subject 31468.895
GSM24658A3243G-MELAS subject 4609.293
GSM24659A3243G-PEO subject 156295
GSM24660A3243G-PEO subject 2557.593
GSM24661A3243G-PEO subject 3710.596
GSM24662A3243G-PEO subject 4707.795
GSM24663mtDNA "Common"-deletion subject 1857.295
GSM24664mtDNA "Common"-deletion subject 21565.295
GSM24665mtDNA "Common"-deletion subject 3110693
GSM24666mtDNA "Common"-deletion subject 41479.795