ProfileGDS1065 / 205243_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 32% 24% 24% 48% 47% 54% 45% 53% 46% 28% 28% 57% 28% 45% 33% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 119.532
GSM24653Normal subject 211.524
GSM24654Normal subject 31324
GSM24655A3243G-MELAS subject 129.648
GSM24656A3243G-MELAS subject 241.847
GSM24657A3243G-MELAS subject 377.654
GSM24658A3243G-MELAS subject 431.445
GSM24659A3243G-PEO subject 141.353
GSM24660A3243G-PEO subject 234.846
GSM24661A3243G-PEO subject 310.728
GSM24662A3243G-PEO subject 412.928
GSM24663mtDNA "Common"-deletion subject 159.857
GSM24664mtDNA "Common"-deletion subject 228.728
GSM24665mtDNA "Common"-deletion subject 353.345
GSM24666mtDNA "Common"-deletion subject 429.733