ProfileGDS1065 / 201667_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 76% 78% 69% 82% 78% 80% 83% 76% 72% 75% 77% 68% 74% 79% 81% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1142.676
GSM24653Normal subject 2147.878
GSM24654Normal subject 3126.569
GSM24655A3243G-MELAS subject 1125.482
GSM24656A3243G-MELAS subject 2155.778
GSM24657A3243G-MELAS subject 3283.180
GSM24658A3243G-MELAS subject 4204.683
GSM24659A3243G-PEO subject 1103.676
GSM24660A3243G-PEO subject 2100.572
GSM24661A3243G-PEO subject 389.675
GSM24662A3243G-PEO subject 4121.477
GSM24663mtDNA "Common"-deletion subject 198.668
GSM24664mtDNA "Common"-deletion subject 2223.674
GSM24665mtDNA "Common"-deletion subject 3266.179
GSM24666mtDNA "Common"-deletion subject 4343.181