ProfileGDS1065 / 212928_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 58% 69% 66% 74% 71% 69% 68% 66% 60% 65% 65% 74% 75% 69% 71% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 162.858
GSM24653Normal subject 29669
GSM24654Normal subject 3106.766
GSM24655A3243G-MELAS subject 183.674
GSM24656A3243G-MELAS subject 2110.771
GSM24657A3243G-MELAS subject 3156.469
GSM24658A3243G-MELAS subject 488.468
GSM24659A3243G-PEO subject 16966
GSM24660A3243G-PEO subject 261.760
GSM24661A3243G-PEO subject 356.465
GSM24662A3243G-PEO subject 468.965
GSM24663mtDNA "Common"-deletion subject 1132.574
GSM24664mtDNA "Common"-deletion subject 2240.375
GSM24665mtDNA "Common"-deletion subject 3149.569
GSM24666mtDNA "Common"-deletion subject 4187.271