ProfileGDS1065 / 218123_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 68% 75% 74% 65% 72% 77% 78% 43% 69% 61% 43% 74% 79% 73% 75% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 195.868
GSM24653Normal subject 2130.175
GSM24654Normal subject 315974
GSM24655A3243G-MELAS subject 155.365
GSM24656A3243G-MELAS subject 2116.272
GSM24657A3243G-MELAS subject 3238.777
GSM24658A3243G-MELAS subject 4154.178
GSM24659A3243G-PEO subject 129.143
GSM24660A3243G-PEO subject 28869
GSM24661A3243G-PEO subject 349.461
GSM24662A3243G-PEO subject 428.843
GSM24663mtDNA "Common"-deletion subject 1134.274
GSM24664mtDNA "Common"-deletion subject 2311.179
GSM24665mtDNA "Common"-deletion subject 3183.273
GSM24666mtDNA "Common"-deletion subject 4223.875