ProfileGDS1065 / 204962_s_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 32% 32% 31% 35% 16% 17% 25% 19% 22% 22% 6% 34% 29% 25% 23% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 11932
GSM24653Normal subject 219.432
GSM24654Normal subject 320.431
GSM24655A3243G-MELAS subject 117.935
GSM24656A3243G-MELAS subject 27.716
GSM24657A3243G-MELAS subject 39.617
GSM24658A3243G-MELAS subject 410.625
GSM24659A3243G-PEO subject 18.319
GSM24660A3243G-PEO subject 210.422
GSM24661A3243G-PEO subject 37.422
GSM24662A3243G-PEO subject 42.66
GSM24663mtDNA "Common"-deletion subject 120.934
GSM24664mtDNA "Common"-deletion subject 229.929
GSM24665mtDNA "Common"-deletion subject 318.425
GSM24666mtDNA "Common"-deletion subject 415.523