ProfileGDS1065 / 218905_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 74% 79% 65% 67% 58% 75% 71% 66% 63% 61% 64% 68% 81% 78% 81% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1131.174
GSM24653Normal subject 2157.679
GSM24654Normal subject 3100.565
GSM24655A3243G-MELAS subject 160.767
GSM24656A3243G-MELAS subject 263.658
GSM24657A3243G-MELAS subject 3208.875
GSM24658A3243G-MELAS subject 4102.971
GSM24659A3243G-PEO subject 168.466
GSM24660A3243G-PEO subject 267.563
GSM24661A3243G-PEO subject 34861
GSM24662A3243G-PEO subject 46764
GSM24663mtDNA "Common"-deletion subject 199.268
GSM24664mtDNA "Common"-deletion subject 2342.881
GSM24665mtDNA "Common"-deletion subject 325178
GSM24666mtDNA "Common"-deletion subject 4333.381