ProfileGDS1065 / 204894_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 71% 80% 68% 63% 82% 73% 81% 60% 74% 66% 73% 54% 69% 71% 70% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1109.971
GSM24653Normal subject 2174.780
GSM24654Normal subject 3117.568
GSM24655A3243G-MELAS subject 152.463
GSM24656A3243G-MELAS subject 2199.882
GSM24657A3243G-MELAS subject 3189.873
GSM24658A3243G-MELAS subject 4179.981
GSM24659A3243G-PEO subject 153.560
GSM24660A3243G-PEO subject 2109.874
GSM24661A3243G-PEO subject 359.666
GSM24662A3243G-PEO subject 497.773
GSM24663mtDNA "Common"-deletion subject 153.354
GSM24664mtDNA "Common"-deletion subject 2173.269
GSM24665mtDNA "Common"-deletion subject 3163.271
GSM24666mtDNA "Common"-deletion subject 4173.970