ProfileGDS1065 / 211759_x_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% 91% 93% 86% 91% 91% 90% 92% 93% 91% 95% 92% 90% 86% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 150691
GSM24653Normal subject 2541.893
GSM24654Normal subject 3585.791
GSM24655A3243G-MELAS subject 1359.693
GSM24656A3243G-MELAS subject 2278.286
GSM24657A3243G-MELAS subject 3778.691
GSM24658A3243G-MELAS subject 4454.691
GSM24659A3243G-PEO subject 128090
GSM24660A3243G-PEO subject 243092
GSM24661A3243G-PEO subject 3420.393
GSM24662A3243G-PEO subject 4362.691
GSM24663mtDNA "Common"-deletion subject 1878.495
GSM24664mtDNA "Common"-deletion subject 2887.492
GSM24665mtDNA "Common"-deletion subject 3642.490
GSM24666mtDNA "Common"-deletion subject 4503.486