ProfileGDS1065 / 211769_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 75% 73% 87% 80% 83% 78% 83% 65% 78% 68% 67% 75% 82% 80% 81% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1136.475
GSM24653Normal subject 2113.673
GSM24654Normal subject 3400.387
GSM24655A3243G-MELAS subject 1114.780
GSM24656A3243G-MELAS subject 2212.983
GSM24657A3243G-MELAS subject 3245.978
GSM24658A3243G-MELAS subject 4200.283
GSM24659A3243G-PEO subject 166.465
GSM24660A3243G-PEO subject 2136.278
GSM24661A3243G-PEO subject 366.668
GSM24662A3243G-PEO subject 474.167
GSM24663mtDNA "Common"-deletion subject 114175
GSM24664mtDNA "Common"-deletion subject 2366.282
GSM24665mtDNA "Common"-deletion subject 3276.880
GSM24666mtDNA "Common"-deletion subject 4341.681