ProfileGDS1065 / 36907_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 87% 85% 86% 85% 85% 82% 83% 90% 86% 83% 85% 88% 86% 81% 83% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1309.387
GSM24653Normal subject 2240.785
GSM24654Normal subject 3368.186
GSM24655A3243G-MELAS subject 115685
GSM24656A3243G-MELAS subject 2241.785
GSM24657A3243G-MELAS subject 3333.282
GSM24658A3243G-MELAS subject 420883
GSM24659A3243G-PEO subject 1286.690
GSM24660A3243G-PEO subject 2246.886
GSM24661A3243G-PEO subject 3154.783
GSM24662A3243G-PEO subject 4212.985
GSM24663mtDNA "Common"-deletion subject 1340.388
GSM24664mtDNA "Common"-deletion subject 2495.986
GSM24665mtDNA "Common"-deletion subject 3308.181
GSM24666mtDNA "Common"-deletion subject 4380.283