ProfileGDS1065 / 209337_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 80% 88% 87% 84% 84% 83% 81% 72% 76% 79% 75% 75% 89% 84% 87% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1179.680
GSM24653Normal subject 2300.788
GSM24654Normal subject 337687
GSM24655A3243G-MELAS subject 1145.784
GSM24656A3243G-MELAS subject 2237.484
GSM24657A3243G-MELAS subject 3346.483
GSM24658A3243G-MELAS subject 4184.381
GSM24659A3243G-PEO subject 188.372
GSM24660A3243G-PEO subject 2120.676
GSM24661A3243G-PEO subject 3113.779
GSM24662A3243G-PEO subject 4111.975
GSM24663mtDNA "Common"-deletion subject 1141.175
GSM24664mtDNA "Common"-deletion subject 2614.189
GSM24665mtDNA "Common"-deletion subject 336784
GSM24666mtDNA "Common"-deletion subject 4533.187