ProfileGDS1065 / 217861_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 82% 89% 85% 91% 88% 90% 90% 89% 87% 85% 85% 87% 89% 83% 83% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1206.182
GSM24653Normal subject 2335.889
GSM24654Normal subject 3317.885
GSM24655A3243G-MELAS subject 1283.591
GSM24656A3243G-MELAS subject 2305.588
GSM24657A3243G-MELAS subject 3639.390
GSM24658A3243G-MELAS subject 4378.190
GSM24659A3243G-PEO subject 1248.889
GSM24660A3243G-PEO subject 2265.387
GSM24661A3243G-PEO subject 3170.385
GSM24662A3243G-PEO subject 420985
GSM24663mtDNA "Common"-deletion subject 1311.987
GSM24664mtDNA "Common"-deletion subject 2621.789
GSM24665mtDNA "Common"-deletion subject 3345.383
GSM24666mtDNA "Common"-deletion subject 4395.983