ProfileGDS1065 / 207475_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 26% 31% 33% 56% 27% 30% 11% 28% 24% 37% 16% 38% 28% 33% 8% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 113.526
GSM24653Normal subject 218.331
GSM24654Normal subject 324.533
GSM24655A3243G-MELAS subject 140.756
GSM24656A3243G-MELAS subject 216.527
GSM24657A3243G-MELAS subject 323.930
GSM24658A3243G-MELAS subject 43.811
GSM24659A3243G-PEO subject 114.428
GSM24660A3243G-PEO subject 211.924
GSM24661A3243G-PEO subject 317.337
GSM24662A3243G-PEO subject 45.816
GSM24663mtDNA "Common"-deletion subject 127.138
GSM24664mtDNA "Common"-deletion subject 228.228
GSM24665mtDNA "Common"-deletion subject 330.133
GSM24666mtDNA "Common"-deletion subject 44.48