ProfileGDS1065 / 121_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% 90% 90% 91% 92% 88% 90% 92% 93% 90% 91% 92% 90% 91% 88% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1484.391
GSM24653Normal subject 2390.390
GSM24654Normal subject 3506.190
GSM24655A3243G-MELAS subject 1278.591
GSM24656A3243G-MELAS subject 2483.892
GSM24657A3243G-MELAS subject 3559.388
GSM24658A3243G-MELAS subject 4373.290
GSM24659A3243G-PEO subject 1340.992
GSM24660A3243G-PEO subject 2493.493
GSM24661A3243G-PEO subject 328690
GSM24662A3243G-PEO subject 4355.591
GSM24663mtDNA "Common"-deletion subject 1556.392
GSM24664mtDNA "Common"-deletion subject 2706.890
GSM24665mtDNA "Common"-deletion subject 3721.691
GSM24666mtDNA "Common"-deletion subject 4596.688