ProfileGDS1065 / 216667_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 37% 18% 22% 41% 25% 15% 16% 34% 15% 18% 14% 20% 35% 21% 20% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 125.837
GSM24653Normal subject 27.818
GSM24654Normal subject 311.622
GSM24655A3243G-MELAS subject 123.241
GSM24656A3243G-MELAS subject 213.825
GSM24657A3243G-MELAS subject 37.915
GSM24658A3243G-MELAS subject 45.516
GSM24659A3243G-PEO subject 118.934
GSM24660A3243G-PEO subject 26.315
GSM24661A3243G-PEO subject 35.518
GSM24662A3243G-PEO subject 45.214
GSM24663mtDNA "Common"-deletion subject 18.720
GSM24664mtDNA "Common"-deletion subject 241.535
GSM24665mtDNA "Common"-deletion subject 314.221
GSM24666mtDNA "Common"-deletion subject 412.520