ProfileGDS1065 / 216239_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 21% 8% 28% 25% 28% 20% 27% 21% 17% 10% 4% 13% 18% 35% 29% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 19.921
GSM24653Normal subject 23.48
GSM24654Normal subject 316.828
GSM24655A3243G-MELAS subject 110.325
GSM24656A3243G-MELAS subject 217.128
GSM24657A3243G-MELAS subject 312.320
GSM24658A3243G-MELAS subject 412.127
GSM24659A3243G-PEO subject 19.121
GSM24660A3243G-PEO subject 27.117
GSM24661A3243G-PEO subject 33.310
GSM24662A3243G-PEO subject 41.94
GSM24663mtDNA "Common"-deletion subject 15.413
GSM24664mtDNA "Common"-deletion subject 213.618
GSM24665mtDNA "Common"-deletion subject 332.735
GSM24666mtDNA "Common"-deletion subject 423.129