ProfileGDS1065 / 217772_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 93% 92% 94% 93% 92% 91% 89% 94% 91% 94% 94% 94% 88% 92% 89% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1687.393
GSM24653Normal subject 2481.892
GSM24654Normal subject 3961.494
GSM24655A3243G-MELAS subject 1347.493
GSM24656A3243G-MELAS subject 2486.292
GSM24657A3243G-MELAS subject 3752.991
GSM24658A3243G-MELAS subject 4345.189
GSM24659A3243G-PEO subject 1492.194
GSM24660A3243G-PEO subject 2413.291
GSM24661A3243G-PEO subject 3521.294
GSM24662A3243G-PEO subject 4609.794
GSM24663mtDNA "Common"-deletion subject 171794
GSM24664mtDNA "Common"-deletion subject 2594.688
GSM24665mtDNA "Common"-deletion subject 3923.792
GSM24666mtDNA "Common"-deletion subject 4674.689