ProfileGDS1065 / 211204_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 22% 21% 36% 36% 21% 47% 9% 37% 45% 28% 46% 29% 25% 24% 37% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 110.422
GSM24653Normal subject 29.421
GSM24654Normal subject 328.136
GSM24655A3243G-MELAS subject 118.436
GSM24656A3243G-MELAS subject 210.521
GSM24657A3243G-MELAS subject 356.947
GSM24658A3243G-MELAS subject 43.19
GSM24659A3243G-PEO subject 122.637
GSM24660A3243G-PEO subject 233.545
GSM24661A3243G-PEO subject 310.728
GSM24662A3243G-PEO subject 431.546
GSM24663mtDNA "Common"-deletion subject 11629
GSM24664mtDNA "Common"-deletion subject 222.425
GSM24665mtDNA "Common"-deletion subject 316.524
GSM24666mtDNA "Common"-deletion subject 436.737