ProfileGDS1065 / 202690_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 78% 83% 74% 79% 82% 87% 83% 82% 78% 85% 81% 75% 78% 80% 82% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1166.778
GSM24653Normal subject 2210.183
GSM24654Normal subject 3160.274
GSM24655A3243G-MELAS subject 1105.479
GSM24656A3243G-MELAS subject 2200.882
GSM24657A3243G-MELAS subject 348587
GSM24658A3243G-MELAS subject 420983
GSM24659A3243G-PEO subject 1144.282
GSM24660A3243G-PEO subject 2141.778
GSM24661A3243G-PEO subject 3174.985
GSM24662A3243G-PEO subject 4161.781
GSM24663mtDNA "Common"-deletion subject 1142.475
GSM24664mtDNA "Common"-deletion subject 228078
GSM24665mtDNA "Common"-deletion subject 328680
GSM24666mtDNA "Common"-deletion subject 4357.682