ProfileGDS1065 / 217397_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 47% 57% 51% 38% 50% 44% 51% 47% 50% 46% 41% 54% 57% 47% 52% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 139.747
GSM24653Normal subject 255.557
GSM24654Normal subject 356.351
GSM24655A3243G-MELAS subject 120.538
GSM24656A3243G-MELAS subject 247.950
GSM24657A3243G-MELAS subject 350.244
GSM24658A3243G-MELAS subject 440.651
GSM24659A3243G-PEO subject 133.447
GSM24660A3243G-PEO subject 241.250
GSM24661A3243G-PEO subject 326.646
GSM24662A3243G-PEO subject 425.741
GSM24663mtDNA "Common"-deletion subject 154.254
GSM24664mtDNA "Common"-deletion subject 2103.857
GSM24665mtDNA "Common"-deletion subject 357.947
GSM24666mtDNA "Common"-deletion subject 471.752