ProfileGDS1065 / 205101_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 35% 35% 14% 24% 1% 46% 39% 15% 10% 49% 45% 34% 30% 10% 33% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 122.735
GSM24653Normal subject 221.935
GSM24654Normal subject 36.414
GSM24655A3243G-MELAS subject 19.124
GSM24656A3243G-MELAS subject 21.21
GSM24657A3243G-MELAS subject 354.146
GSM24658A3243G-MELAS subject 424.639
GSM24659A3243G-PEO subject 16.415
GSM24660A3243G-PEO subject 24.210
GSM24661A3243G-PEO subject 330.749
GSM24662A3243G-PEO subject 430.345
GSM24663mtDNA "Common"-deletion subject 121.834
GSM24664mtDNA "Common"-deletion subject 230.930
GSM24665mtDNA "Common"-deletion subject 36.110
GSM24666mtDNA "Common"-deletion subject 429.533