ProfileGDS1065 / 220610_s_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 75% 63% 77% 76% 74% 67% 72% 64% 73% 68% 74% 71% 65% 72% 63% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1137.175
GSM24653Normal subject 271.463
GSM24654Normal subject 3189.377
GSM24655A3243G-MELAS subject 192.176
GSM24656A3243G-MELAS subject 213074
GSM24657A3243G-MELAS subject 3138.667
GSM24658A3243G-MELAS subject 4109.872
GSM24659A3243G-PEO subject 16464
GSM24660A3243G-PEO subject 2105.773
GSM24661A3243G-PEO subject 367.468
GSM24662A3243G-PEO subject 4105.474
GSM24663mtDNA "Common"-deletion subject 1112.971
GSM24664mtDNA "Common"-deletion subject 2146.165
GSM24665mtDNA "Common"-deletion subject 3171.272
GSM24666mtDNA "Common"-deletion subject 4118.563