ProfileGDS1065 / 203258_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 82% 65% 81% 69% 78% 68% 68% 74% 66% 72% 73% 67% 67% 79% 65% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1214.882
GSM24653Normal subject 278.565
GSM24654Normal subject 3240.981
GSM24655A3243G-MELAS subject 167.769
GSM24656A3243G-MELAS subject 2157.778
GSM24657A3243G-MELAS subject 3147.568
GSM24658A3243G-MELAS subject 48868
GSM24659A3243G-PEO subject 196.774
GSM24660A3243G-PEO subject 279.566
GSM24661A3243G-PEO subject 37872
GSM24662A3243G-PEO subject 4100.373
GSM24663mtDNA "Common"-deletion subject 192.167
GSM24664mtDNA "Common"-deletion subject 2158.667
GSM24665mtDNA "Common"-deletion subject 3259.379
GSM24666mtDNA "Common"-deletion subject 4133.565