ProfileGDS1065 / 213016_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 58% 62% 71% 58% 67% 59% 72% 49% 60% 51% 55% 64% 53% 58% 65% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 162.358
GSM24653Normal subject 267.462
GSM24654Normal subject 3138.371
GSM24655A3243G-MELAS subject 143.358
GSM24656A3243G-MELAS subject 291.767
GSM24657A3243G-MELAS subject 394.659
GSM24658A3243G-MELAS subject 4109.272
GSM24659A3243G-PEO subject 135.949
GSM24660A3243G-PEO subject 259.860
GSM24661A3243G-PEO subject 333.251
GSM24662A3243G-PEO subject 446.555
GSM24663mtDNA "Common"-deletion subject 183.164
GSM24664mtDNA "Common"-deletion subject 288.353
GSM24665mtDNA "Common"-deletion subject 390.558
GSM24666mtDNA "Common"-deletion subject 4129.665