ProfileGDS1065 / 206833_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 91% 93% 94% 94% 94% 90% 91% 92% 92% 91% 87% 90% 92% 94% 92% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1497.691
GSM24653Normal subject 2555.493
GSM24654Normal subject 3966.794
GSM24655A3243G-MELAS subject 1423.194
GSM24656A3243G-MELAS subject 2684.894
GSM24657A3243G-MELAS subject 365990
GSM24658A3243G-MELAS subject 4454.291
GSM24659A3243G-PEO subject 1348.992
GSM24660A3243G-PEO subject 2486.892
GSM24661A3243G-PEO subject 3313.491
GSM24662A3243G-PEO subject 4238.787
GSM24663mtDNA "Common"-deletion subject 1432.490
GSM24664mtDNA "Common"-deletion subject 2960.892
GSM24665mtDNA "Common"-deletion subject 31306.594
GSM24666mtDNA "Common"-deletion subject 4992.692