ProfileGDS1065 / 202181_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 78% 81% 79% 78% 78% 75% 74% 74% 78% 73% 50% 73% 71% 75% 80% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1163.778
GSM24653Normal subject 2185.181
GSM24654Normal subject 3218.179
GSM24655A3243G-MELAS subject 110378
GSM24656A3243G-MELAS subject 215778
GSM24657A3243G-MELAS subject 3213.175
GSM24658A3243G-MELAS subject 4121.574
GSM24659A3243G-PEO subject 194.774
GSM24660A3243G-PEO subject 213878
GSM24661A3243G-PEO subject 381.173
GSM24662A3243G-PEO subject 43850
GSM24663mtDNA "Common"-deletion subject 1124.873
GSM24664mtDNA "Common"-deletion subject 2193.671
GSM24665mtDNA "Common"-deletion subject 3210.275
GSM24666mtDNA "Common"-deletion subject 4314.180