ProfileGDS1065 / 220693_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 28% 42% 33% 32% 40% 29% 35% 34% 32% 25% 35% 26% 24% 36% 31% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 115.228
GSM24653Normal subject 231.242
GSM24654Normal subject 324.233
GSM24655A3243G-MELAS subject 114.732
GSM24656A3243G-MELAS subject 230.940
GSM24657A3243G-MELAS subject 322.929
GSM24658A3243G-MELAS subject 419.535
GSM24659A3243G-PEO subject 119.334
GSM24660A3243G-PEO subject 218.832
GSM24661A3243G-PEO subject 38.525
GSM24662A3243G-PEO subject 419.735
GSM24663mtDNA "Common"-deletion subject 113.526
GSM24664mtDNA "Common"-deletion subject 220.824
GSM24665mtDNA "Common"-deletion subject 334.836
GSM24666mtDNA "Common"-deletion subject 426.531