ProfileGDS1065 / 205933_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 86% 75% 80% 73% 85% 82% 86% 84% 85% 85% 80% 82% 81% 86% 88% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1292.686
GSM24653Normal subject 2126.975
GSM24654Normal subject 3222.680
GSM24655A3243G-MELAS subject 18073
GSM24656A3243G-MELAS subject 2244.985
GSM24657A3243G-MELAS subject 3340.282
GSM24658A3243G-MELAS subject 4251.286
GSM24659A3243G-PEO subject 1163.484
GSM24660A3243G-PEO subject 2227.285
GSM24661A3243G-PEO subject 3173.685
GSM24662A3243G-PEO subject 4145.580
GSM24663mtDNA "Common"-deletion subject 1212.582
GSM24664mtDNA "Common"-deletion subject 2342.781
GSM24665mtDNA "Common"-deletion subject 3457.186
GSM24666mtDNA "Common"-deletion subject 461688