ProfileGDS1065 / 221818_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 73% 63% 67% 50% 72% 65% 68% 61% 76% 68% 78% 68% 71% 66% 66% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1121.373
GSM24653Normal subject 270.463
GSM24654Normal subject 3114.967
GSM24655A3243G-MELAS subject 132.650
GSM24656A3243G-MELAS subject 2113.672
GSM24657A3243G-MELAS subject 312665
GSM24658A3243G-MELAS subject 489.268
GSM24659A3243G-PEO subject 156.161
GSM24660A3243G-PEO subject 2124.576
GSM24661A3243G-PEO subject 367.568
GSM24662A3243G-PEO subject 4130.178
GSM24663mtDNA "Common"-deletion subject 198.768
GSM24664mtDNA "Common"-deletion subject 2189.671
GSM24665mtDNA "Common"-deletion subject 3129.366
GSM24666mtDNA "Common"-deletion subject 4138.966