ProfileGDS1065 / 217853_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 71% 87% 76% 86% 77% 85% 85% 82% 79% 84% 82% 84% 86% 85% 83% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1112.671
GSM24653Normal subject 2288.287
GSM24654Normal subject 3184.276
GSM24655A3243G-MELAS subject 1174.986
GSM24656A3243G-MELAS subject 2150.677
GSM24657A3243G-MELAS subject 3413.485
GSM24658A3243G-MELAS subject 4242.385
GSM24659A3243G-PEO subject 1147.782
GSM24660A3243G-PEO subject 2147.279
GSM24661A3243G-PEO subject 3162.484
GSM24662A3243G-PEO subject 4164.382
GSM24663mtDNA "Common"-deletion subject 125684
GSM24664mtDNA "Common"-deletion subject 2477.886
GSM24665mtDNA "Common"-deletion subject 3402.885
GSM24666mtDNA "Common"-deletion subject 4391.583