ProfileGDS1065 / 206074_s_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 88% 77% 83% 79% 86% 86% 81% 86% 90% 89% 88% 84% 87% 85% 86% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1355.188
GSM24653Normal subject 2144.277
GSM24654Normal subject 3280.483
GSM24655A3243G-MELAS subject 1107.179
GSM24656A3243G-MELAS subject 2279.686
GSM24657A3243G-MELAS subject 345186
GSM24658A3243G-MELAS subject 4184.781
GSM24659A3243G-PEO subject 1194.286
GSM24660A3243G-PEO subject 234890
GSM24661A3243G-PEO subject 3254.589
GSM24662A3243G-PEO subject 4276.788
GSM24663mtDNA "Common"-deletion subject 1254.484
GSM24664mtDNA "Common"-deletion subject 2533.987
GSM24665mtDNA "Common"-deletion subject 3409.485
GSM24666mtDNA "Common"-deletion subject 447886