ProfileGDS1065 / 211945_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 94% 95% 95% 96% 96% 94% 94% 93% 94% 93% 92% 94% 96% 95% 96% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1786.594
GSM24653Normal subject 2777.195
GSM24654Normal subject 31296.295
GSM24655A3243G-MELAS subject 1691.596
GSM24656A3243G-MELAS subject 21126.696
GSM24657A3243G-MELAS subject 31252.394
GSM24658A3243G-MELAS subject 4719.694
GSM24659A3243G-PEO subject 1436.493
GSM24660A3243G-PEO subject 2675.194
GSM24661A3243G-PEO subject 3435.493
GSM24662A3243G-PEO subject 4448.892
GSM24663mtDNA "Common"-deletion subject 1769.594
GSM24664mtDNA "Common"-deletion subject 21908.496
GSM24665mtDNA "Common"-deletion subject 31600.395
GSM24666mtDNA "Common"-deletion subject 41868.596