ProfileGDS1065 / 213857_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% 85% 78% 86% 75% 86% 82% 82% 82% 86% 89% 85% 85% 80% 87% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1135.375
GSM24653Normal subject 2244.285
GSM24654Normal subject 3207.978
GSM24655A3243G-MELAS subject 1167.486
GSM24656A3243G-MELAS subject 2131.175
GSM24657A3243G-MELAS subject 3441.686
GSM24658A3243G-MELAS subject 4189.282
GSM24659A3243G-PEO subject 1150.182
GSM24660A3243G-PEO subject 2179.582
GSM24661A3243G-PEO subject 3189.786
GSM24662A3243G-PEO subject 4286.389
GSM24663mtDNA "Common"-deletion subject 1274.685
GSM24664mtDNA "Common"-deletion subject 2465.585
GSM24665mtDNA "Common"-deletion subject 3274.480
GSM24666mtDNA "Common"-deletion subject 4538.787