ProfileGDS1065 / 201153_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 96% 96% 96% 96% 97% 96% 96% 96% 96% 95% 95% 96% 96% 96% 97% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 11414.196
GSM24653Normal subject 21016.296
GSM24654Normal subject 31598.896
GSM24655A3243G-MELAS subject 1634.296
GSM24656A3243G-MELAS subject 21564.697
GSM24657A3243G-MELAS subject 3188396
GSM24658A3243G-MELAS subject 41177.896
GSM24659A3243G-PEO subject 1682.496
GSM24660A3243G-PEO subject 21094.796
GSM24661A3243G-PEO subject 3592.895
GSM24662A3243G-PEO subject 4756.195
GSM24663mtDNA "Common"-deletion subject 11108.496
GSM24664mtDNA "Common"-deletion subject 22142.796
GSM24665mtDNA "Common"-deletion subject 32152.196
GSM24666mtDNA "Common"-deletion subject 4330997