ProfileGDS1065 / 215562_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 34% 29% 19% 35% 25% 25% 22% 22% 27% 24% 27% 15% 36% 30% 16% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 121.434
GSM24653Normal subject 216.429
GSM24654Normal subject 39.419
GSM24655A3243G-MELAS subject 117.335
GSM24656A3243G-MELAS subject 214.225
GSM24657A3243G-MELAS subject 317.225
GSM24658A3243G-MELAS subject 48.722
GSM24659A3243G-PEO subject 19.922
GSM24660A3243G-PEO subject 213.627
GSM24661A3243G-PEO subject 38.224
GSM24662A3243G-PEO subject 412.727
GSM24663mtDNA "Common"-deletion subject 16.315
GSM24664mtDNA "Common"-deletion subject 243.836
GSM24665mtDNA "Common"-deletion subject 325.330
GSM24666mtDNA "Common"-deletion subject 48.816