ProfileGDS1065 / 214287_s_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 42% 43% 36% 29% 40% 23% 14% 59% 40% 30% 52% 52% 36% 41% 43% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 131.742
GSM24653Normal subject 232.443
GSM24654Normal subject 328.136
GSM24655A3243G-MELAS subject 112.429
GSM24656A3243G-MELAS subject 231.440
GSM24657A3243G-MELAS subject 314.923
GSM24658A3243G-MELAS subject 44.814
GSM24659A3243G-PEO subject 152.159
GSM24660A3243G-PEO subject 227.440
GSM24661A3243G-PEO subject 311.730
GSM24662A3243G-PEO subject 440.452
GSM24663mtDNA "Common"-deletion subject 149.852
GSM24664mtDNA "Common"-deletion subject 243.536
GSM24665mtDNA "Common"-deletion subject 344.441
GSM24666mtDNA "Common"-deletion subject 449.543