ProfileGDS1065 / 202117_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 85% 88% 83% 91% 87% 89% 87% 90% 88% 89% 90% 86% 85% 82% 84% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1269.585
GSM24653Normal subject 229888
GSM24654Normal subject 3288.383
GSM24655A3243G-MELAS subject 1267.591
GSM24656A3243G-MELAS subject 2289.387
GSM24657A3243G-MELAS subject 3581.489
GSM24658A3243G-MELAS subject 4280.487
GSM24659A3243G-PEO subject 1275.890
GSM24660A3243G-PEO subject 2283.688
GSM24661A3243G-PEO subject 3246.489
GSM24662A3243G-PEO subject 433590
GSM24663mtDNA "Common"-deletion subject 1286.686
GSM24664mtDNA "Common"-deletion subject 2464.185
GSM24665mtDNA "Common"-deletion subject 3320.282
GSM24666mtDNA "Common"-deletion subject 4413.684