ProfileGDS1065 / 213992_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 41% 43% 40% 45% 45% 39% 39% 36% 46% 31% 43% 35% 57% 47% 51% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 130.441
GSM24653Normal subject 232.543
GSM24654Normal subject 333.440
GSM24655A3243G-MELAS subject 127.245
GSM24656A3243G-MELAS subject 239.345
GSM24657A3243G-MELAS subject 338.739
GSM24658A3243G-MELAS subject 424.539
GSM24659A3243G-PEO subject 121.536
GSM24660A3243G-PEO subject 235.546
GSM24661A3243G-PEO subject 312.731
GSM24662A3243G-PEO subject 428.643
GSM24663mtDNA "Common"-deletion subject 122.335
GSM24664mtDNA "Common"-deletion subject 2104.557
GSM24665mtDNA "Common"-deletion subject 358.247
GSM24666mtDNA "Common"-deletion subject 470.451