ProfileGDS1065 / 201976_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 69% 73% 54% 75% 68% 77% 72% 66% 68% 63% 70% 69% 71% 64% 69% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 199.469
GSM24653Normal subject 2111.573
GSM24654Normal subject 363.554
GSM24655A3243G-MELAS subject 185.475
GSM24656A3243G-MELAS subject 294.668
GSM24657A3243G-MELAS subject 3245.477
GSM24658A3243G-MELAS subject 411072
GSM24659A3243G-PEO subject 168.366
GSM24660A3243G-PEO subject 285.168
GSM24661A3243G-PEO subject 352.263
GSM24662A3243G-PEO subject 48670
GSM24663mtDNA "Common"-deletion subject 1104.869
GSM24664mtDNA "Common"-deletion subject 2196.671
GSM24665mtDNA "Common"-deletion subject 3118.364
GSM24666mtDNA "Common"-deletion subject 4166.869