ProfileGDS1065 / 204749_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 7% 35% 37% 44% 28% 35% 37% 41% 30% 31% 27% 38% 38% 34% 44% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 13.47
GSM24653Normal subject 221.835
GSM24654Normal subject 329.937
GSM24655A3243G-MELAS subject 126.244
GSM24656A3243G-MELAS subject 217.128
GSM24657A3243G-MELAS subject 331.535
GSM24658A3243G-MELAS subject 42237
GSM24659A3243G-PEO subject 126.341
GSM24660A3243G-PEO subject 216.130
GSM24661A3243G-PEO subject 312.831
GSM24662A3243G-PEO subject 412.227
GSM24663mtDNA "Common"-deletion subject 126.338
GSM24664mtDNA "Common"-deletion subject 247.238
GSM24665mtDNA "Common"-deletion subject 331.534
GSM24666mtDNA "Common"-deletion subject 450.544