ProfileGDS1065 / 214679_x_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% 80% 82% 83% 83% 81% 82% 78% 84% 79% 78% 83% 79% 83% 82% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1211.182
GSM24653Normal subject 2166.880
GSM24654Normal subject 3268.182
GSM24655A3243G-MELAS subject 1131.783
GSM24656A3243G-MELAS subject 2214.283
GSM24657A3243G-MELAS subject 3308.981
GSM24658A3243G-MELAS subject 4193.582
GSM24659A3243G-PEO subject 1116.178
GSM24660A3243G-PEO subject 220184
GSM24661A3243G-PEO subject 311979
GSM24662A3243G-PEO subject 4134.778
GSM24663mtDNA "Common"-deletion subject 123583
GSM24664mtDNA "Common"-deletion subject 230879
GSM24665mtDNA "Common"-deletion subject 3336.183
GSM24666mtDNA "Common"-deletion subject 4363.582