ProfileGDS1065 / 201362_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 77% 77% 74% 60% 74% 72% 67% 63% 75% 78% 74% 74% 69% 75% 79% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1154.777
GSM24653Normal subject 214077
GSM24654Normal subject 3160.874
GSM24655A3243G-MELAS subject 146.360
GSM24656A3243G-MELAS subject 2130.574
GSM24657A3243G-MELAS subject 3178.472
GSM24658A3243G-MELAS subject 482.267
GSM24659A3243G-PEO subject 16063
GSM24660A3243G-PEO subject 211575
GSM24661A3243G-PEO subject 3106.778
GSM24662A3243G-PEO subject 4106.274
GSM24663mtDNA "Common"-deletion subject 1131.874
GSM24664mtDNA "Common"-deletion subject 2178.469
GSM24665mtDNA "Common"-deletion subject 3209.575
GSM24666mtDNA "Common"-deletion subject 4299.779