ProfileGDS1065 / 206662_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 88% 97% 90% 94% 87% 96% 92% 88% 88% 90% 82% 87% 91% 91% 93% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1362.588
GSM24653Normal subject 21332.797
GSM24654Normal subject 3546.790
GSM24655A3243G-MELAS subject 1444.894
GSM24656A3243G-MELAS subject 229087
GSM24657A3243G-MELAS subject 31953.796
GSM24658A3243G-MELAS subject 4483.692
GSM24659A3243G-PEO subject 1236.188
GSM24660A3243G-PEO subject 2288.388
GSM24661A3243G-PEO subject 3275.590
GSM24662A3243G-PEO subject 417282
GSM24663mtDNA "Common"-deletion subject 1331.387
GSM24664mtDNA "Common"-deletion subject 2754.291
GSM24665mtDNA "Common"-deletion subject 3768.691
GSM24666mtDNA "Common"-deletion subject 4104693