ProfileGDS1065 / 205749_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 30% 42% 33% 60% 41% 80% 45% 61% 38% 46% 36% 48% 43% 41% 35% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 117.330
GSM24653Normal subject 231.142
GSM24654Normal subject 324.433
GSM24655A3243G-MELAS subject 147.360
GSM24656A3243G-MELAS subject 233.541
GSM24657A3243G-MELAS subject 3286.680
GSM24658A3243G-MELAS subject 431.645
GSM24659A3243G-PEO subject 156.261
GSM24660A3243G-PEO subject 224.838
GSM24661A3243G-PEO subject 326.246
GSM24662A3243G-PEO subject 420.836
GSM24663mtDNA "Common"-deletion subject 141.848
GSM24664mtDNA "Common"-deletion subject 258.243
GSM24665mtDNA "Common"-deletion subject 344.641
GSM24666mtDNA "Common"-deletion subject 433.935