ProfileGDS1065 / 200961_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% 84% 87% 85% 84% 85% 89% 88% 86% 87% 87% 90% 90% 83% 88% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1355.288
GSM24653Normal subject 222884
GSM24654Normal subject 3395.287
GSM24655A3243G-MELAS subject 1154.285
GSM24656A3243G-MELAS subject 2238.684
GSM24657A3243G-MELAS subject 3420.185
GSM24658A3243G-MELAS subject 4330.989
GSM24659A3243G-PEO subject 1222.788
GSM24660A3243G-PEO subject 2239.786
GSM24661A3243G-PEO subject 3204.187
GSM24662A3243G-PEO subject 423587
GSM24663mtDNA "Common"-deletion subject 1412.490
GSM24664mtDNA "Common"-deletion subject 2745.190
GSM24665mtDNA "Common"-deletion subject 3352.783
GSM24666mtDNA "Common"-deletion subject 4597.388