ProfileGDS1065 / 202071_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 90% 89% 85% 90% 90% 89% 90% 88% 92% 90% 92% 88% 89% 91% 90% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1447.490
GSM24653Normal subject 2345.389
GSM24654Normal subject 3321.485
GSM24655A3243G-MELAS subject 1232.690
GSM24656A3243G-MELAS subject 2406.990
GSM24657A3243G-MELAS subject 3602.689
GSM24658A3243G-MELAS subject 4395.890
GSM24659A3243G-PEO subject 1225.188
GSM24660A3243G-PEO subject 2474.992
GSM24661A3243G-PEO subject 3285.290
GSM24662A3243G-PEO subject 4445.292
GSM24663mtDNA "Common"-deletion subject 1345.288
GSM24664mtDNA "Common"-deletion subject 2617.589
GSM24665mtDNA "Common"-deletion subject 3792.491
GSM24666mtDNA "Common"-deletion subject 4751.690