ProfileGDS1065 / 211342_x_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 72% 70% 73% 75% 77% 72% 81% 73% 76% 60% 70% 72% 73% 73% 68% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1118.472
GSM24653Normal subject 296.370
GSM24654Normal subject 3156.573
GSM24655A3243G-MELAS subject 188.375
GSM24656A3243G-MELAS subject 2145.477
GSM24657A3243G-MELAS subject 3180.172
GSM24658A3243G-MELAS subject 417881
GSM24659A3243G-PEO subject 190.973
GSM24660A3243G-PEO subject 2123.776
GSM24661A3243G-PEO subject 347.760
GSM24662A3243G-PEO subject 485.970
GSM24663mtDNA "Common"-deletion subject 1116.472
GSM24664mtDNA "Common"-deletion subject 2216.873
GSM24665mtDNA "Common"-deletion subject 3177.973
GSM24666mtDNA "Common"-deletion subject 4158.868