ProfileGDS1065 / 206625_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 84% 85% 81% 79% 79% 88% 83% 88% 83% 89% 83% 84% 82% 88% 88% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1250.784
GSM24653Normal subject 2233.385
GSM24654Normal subject 3251.281
GSM24655A3243G-MELAS subject 1104.679
GSM24656A3243G-MELAS subject 2171.179
GSM24657A3243G-MELAS subject 3554.388
GSM24658A3243G-MELAS subject 4211.883
GSM24659A3243G-PEO subject 1227.188
GSM24660A3243G-PEO subject 219283
GSM24661A3243G-PEO subject 3239.789
GSM24662A3243G-PEO subject 4175.183
GSM24663mtDNA "Common"-deletion subject 124084
GSM24664mtDNA "Common"-deletion subject 2364.182
GSM24665mtDNA "Common"-deletion subject 3521.288
GSM24666mtDNA "Common"-deletion subject 4605.588