ProfileGDS1065 / 203974_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 84% 88% 87% 88% 89% 81% 84% 79% 84% 80% 83% 86% 92% 90% 89% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1236.484
GSM24653Normal subject 232588
GSM24654Normal subject 3393.987
GSM24655A3243G-MELAS subject 1198.188
GSM24656A3243G-MELAS subject 2339.789
GSM24657A3243G-MELAS subject 3309.581
GSM24658A3243G-MELAS subject 4223.984
GSM24659A3243G-PEO subject 1124.279
GSM24660A3243G-PEO subject 2212.984
GSM24661A3243G-PEO subject 312280
GSM24662A3243G-PEO subject 4182.983
GSM24663mtDNA "Common"-deletion subject 1301.186
GSM24664mtDNA "Common"-deletion subject 2897.992
GSM24665mtDNA "Common"-deletion subject 370890
GSM24666mtDNA "Common"-deletion subject 4656.789