ProfileGDS1065 / 209849_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 76% 76% 83% 80% 71% 72% 76% 76% 74% 73% 74% 80% 79% 78% 73% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1142.876
GSM24653Normal subject 213276
GSM24654Normal subject 3283.883
GSM24655A3243G-MELAS subject 1115.180
GSM24656A3243G-MELAS subject 2109.871
GSM24657A3243G-MELAS subject 3179.172
GSM24658A3243G-MELAS subject 4135.676
GSM24659A3243G-PEO subject 1105.876
GSM24660A3243G-PEO subject 2113.874
GSM24661A3243G-PEO subject 384.773
GSM24662A3243G-PEO subject 4103.674
GSM24663mtDNA "Common"-deletion subject 1195.380
GSM24664mtDNA "Common"-deletion subject 2305.679
GSM24665mtDNA "Common"-deletion subject 3251.878
GSM24666mtDNA "Common"-deletion subject 4200.773