ProfileGDS1065 / 204610_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 92% 89% 85% 93% 87% 93% 90% 95% 94% 93% 94% 94% 85% 84% 86% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1525.692
GSM24653Normal subject 2329.389
GSM24654Normal subject 3337.985
GSM24655A3243G-MELAS subject 1380.393
GSM24656A3243G-MELAS subject 2295.487
GSM24657A3243G-MELAS subject 31038.393
GSM24658A3243G-MELAS subject 4362.290
GSM24659A3243G-PEO subject 1633.595
GSM24660A3243G-PEO subject 2667.594
GSM24661A3243G-PEO subject 3427.893
GSM24662A3243G-PEO subject 4586.894
GSM24663mtDNA "Common"-deletion subject 1731.294
GSM24664mtDNA "Common"-deletion subject 2438.985
GSM24665mtDNA "Common"-deletion subject 3374.984
GSM24666mtDNA "Common"-deletion subject 4489.886