ProfileGDS1065 / 216947_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 1% 1% 17% 16% 20% 18% 1% 21% 29% 4% 24% 24% 21% 22% 26% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 10.91
GSM24653Normal subject 211
GSM24654Normal subject 37.917
GSM24655A3243G-MELAS subject 15.516
GSM24656A3243G-MELAS subject 210.420
GSM24657A3243G-MELAS subject 31018
GSM24658A3243G-MELAS subject 40.71
GSM24659A3243G-PEO subject 19.121
GSM24660A3243G-PEO subject 215.529
GSM24661A3243G-PEO subject 31.64
GSM24662A3243G-PEO subject 410.324
GSM24663mtDNA "Common"-deletion subject 111.324
GSM24664mtDNA "Common"-deletion subject 217.521
GSM24665mtDNA "Common"-deletion subject 314.822
GSM24666mtDNA "Common"-deletion subject 419.726