ProfileGDS1065 / 219112_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 19% 21% 9% 3% 20% 24% 3% 4% 21% 7% 4% 9% 12% 24% 28% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 18.519
GSM24653Normal subject 29.421
GSM24654Normal subject 34.19
GSM24655A3243G-MELAS subject 11.73
GSM24656A3243G-MELAS subject 210.320
GSM24657A3243G-MELAS subject 31624
GSM24658A3243G-MELAS subject 41.63
GSM24659A3243G-PEO subject 12.54
GSM24660A3243G-PEO subject 29.621
GSM24661A3243G-PEO subject 32.37
GSM24662A3243G-PEO subject 424
GSM24663mtDNA "Common"-deletion subject 13.89
GSM24664mtDNA "Common"-deletion subject 29.212
GSM24665mtDNA "Common"-deletion subject 31724
GSM24666mtDNA "Common"-deletion subject 422.128