ProfileGDS1065 / 201723_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 79% 82% 89% 82% 85% 72% 82% 72% 84% 79% 77% 79% 79% 88% 79% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1176.479
GSM24653Normal subject 2191.182
GSM24654Normal subject 347089
GSM24655A3243G-MELAS subject 1128.582
GSM24656A3243G-MELAS subject 2242.585
GSM24657A3243G-MELAS subject 3183.672
GSM24658A3243G-MELAS subject 4197.982
GSM24659A3243G-PEO subject 187.672
GSM24660A3243G-PEO subject 2203.784
GSM24661A3243G-PEO subject 3116.979
GSM24662A3243G-PEO subject 4122.577
GSM24663mtDNA "Common"-deletion subject 1174.379
GSM24664mtDNA "Common"-deletion subject 2294.279
GSM24665mtDNA "Common"-deletion subject 3567.388
GSM24666mtDNA "Common"-deletion subject 4300.479