ProfileGDS1065 / 201397_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 59% 71% 56% 67% 61% 68% 68% 73% 65% 68% 65% 77% 70% 62% 62% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 163.759
GSM24653Normal subject 2105.971
GSM24654Normal subject 368.456
GSM24655A3243G-MELAS subject 16267
GSM24656A3243G-MELAS subject 27161
GSM24657A3243G-MELAS subject 3147.668
GSM24658A3243G-MELAS subject 486.868
GSM24659A3243G-PEO subject 18973
GSM24660A3243G-PEO subject 274.565
GSM24661A3243G-PEO subject 36768
GSM24662A3243G-PEO subject 467.765
GSM24663mtDNA "Common"-deletion subject 1158.777
GSM24664mtDNA "Common"-deletion subject 2182.170
GSM24665mtDNA "Common"-deletion subject 3107.562
GSM24666mtDNA "Common"-deletion subject 4113.262