ProfileGDS1065 / 202191_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 73% 76% 75% 75% 74% 73% 71% 85% 72% 84% 65% 68% 68% 64% 67% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 112273
GSM24653Normal subject 2135.876
GSM24654Normal subject 3168.975
GSM24655A3243G-MELAS subject 187.875
GSM24656A3243G-MELAS subject 2127.174
GSM24657A3243G-MELAS subject 3187.273
GSM24658A3243G-MELAS subject 4104.871
GSM24659A3243G-PEO subject 1182.885
GSM24660A3243G-PEO subject 2103.472
GSM24661A3243G-PEO subject 3158.184
GSM24662A3243G-PEO subject 470.165
GSM24663mtDNA "Common"-deletion subject 198.868
GSM24664mtDNA "Common"-deletion subject 2168.468
GSM24665mtDNA "Common"-deletion subject 3119.164
GSM24666mtDNA "Common"-deletion subject 4149.667