ProfileGDS1065 / 218779_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 56% 53% 44% 57% 54% 45% 31% 47% 56% 37% 61% 59% 55% 50% 52% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 157.956
GSM24653Normal subject 248.953
GSM24654Normal subject 341.344
GSM24655A3243G-MELAS subject 14257
GSM24656A3243G-MELAS subject 255.754
GSM24657A3243G-MELAS subject 350.945
GSM24658A3243G-MELAS subject 41631
GSM24659A3243G-PEO subject 133.247
GSM24660A3243G-PEO subject 252.256
GSM24661A3243G-PEO subject 317.937
GSM24662A3243G-PEO subject 458.261
GSM24663mtDNA "Common"-deletion subject 165.959
GSM24664mtDNA "Common"-deletion subject 295.455
GSM24665mtDNA "Common"-deletion subject 364.850
GSM24666mtDNA "Common"-deletion subject 473.952