ProfileGDS1065 / 200763_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 100% 99% 100% 99% 100% 100% 100% 99% 100% 99% 100% 100% 100% 100% 100% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 112142.4100
GSM24653Normal subject 29167.499
GSM24654Normal subject 311790.1100
GSM24655A3243G-MELAS subject 14951.999
GSM24656A3243G-MELAS subject 27652.6100
GSM24657A3243G-MELAS subject 313032.2100
GSM24658A3243G-MELAS subject 410716.6100
GSM24659A3243G-PEO subject 18318.199
GSM24660A3243G-PEO subject 28686.4100
GSM24661A3243G-PEO subject 37952.299
GSM24662A3243G-PEO subject 411456.7100
GSM24663mtDNA "Common"-deletion subject 113092.3100
GSM24664mtDNA "Common"-deletion subject 212861.5100
GSM24665mtDNA "Common"-deletion subject 313320.4100
GSM24666mtDNA "Common"-deletion subject 415009.8100