ProfileGDS1065 / 204039_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 60% 56% 69% 56% 59% 60% 64% 68% 63% 66% 66% 62% 59% 54% 68% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 168.760
GSM24653Normal subject 254.356
GSM24654Normal subject 312669
GSM24655A3243G-MELAS subject 139.956
GSM24656A3243G-MELAS subject 265.959
GSM24657A3243G-MELAS subject 399.260
GSM24658A3243G-MELAS subject 474.264
GSM24659A3243G-PEO subject 173.668
GSM24660A3243G-PEO subject 269.763
GSM24661A3243G-PEO subject 359.266
GSM24662A3243G-PEO subject 470.866
GSM24663mtDNA "Common"-deletion subject 174.262
GSM24664mtDNA "Common"-deletion subject 2111.859
GSM24665mtDNA "Common"-deletion subject 377.554
GSM24666mtDNA "Common"-deletion subject 415968