ProfileGDS1065 / 217815_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 82% 82% 80% 83% 85% 81% 83% 82% 78% 81% 78% 81% 82% 82% 84% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 121482
GSM24653Normal subject 2191.482
GSM24654Normal subject 3226.180
GSM24655A3243G-MELAS subject 1139.383
GSM24656A3243G-MELAS subject 2252.385
GSM24657A3243G-MELAS subject 3307.181
GSM24658A3243G-MELAS subject 4208.983
GSM24659A3243G-PEO subject 1147.482
GSM24660A3243G-PEO subject 214078
GSM24661A3243G-PEO subject 3136.281
GSM24662A3243G-PEO subject 4129.778
GSM24663mtDNA "Common"-deletion subject 1204.281
GSM24664mtDNA "Common"-deletion subject 2374.582
GSM24665mtDNA "Common"-deletion subject 3330.382
GSM24666mtDNA "Common"-deletion subject 4410.384