ProfileGDS1065 / 219391_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% 31% 16% 15% 4% 8% 2% 13% 9% 26% 2% 18% 16% 18% 4% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 115.528
GSM24653Normal subject 217.731
GSM24654Normal subject 37.416
GSM24655A3243G-MELAS subject 15.115
GSM24656A3243G-MELAS subject 22.84
GSM24657A3243G-MELAS subject 34.38
GSM24658A3243G-MELAS subject 41.22
GSM24659A3243G-PEO subject 15.513
GSM24660A3243G-PEO subject 249
GSM24661A3243G-PEO subject 39.126
GSM24662A3243G-PEO subject 41.42
GSM24663mtDNA "Common"-deletion subject 17.618
GSM24664mtDNA "Common"-deletion subject 212.216
GSM24665mtDNA "Common"-deletion subject 310.618
GSM24666mtDNA "Common"-deletion subject 434