ProfileGDS1065 / 212130_x_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 99% 99% 99% 99% 99% 99% 99% 99% 99% 99% 99% 99% 99% 99% 99% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 18406.699
GSM24653Normal subject 28801.899
GSM24654Normal subject 311063.499
GSM24655A3243G-MELAS subject 14281.999
GSM24656A3243G-MELAS subject 2590999
GSM24657A3243G-MELAS subject 39409.999
GSM24658A3243G-MELAS subject 48324.999
GSM24659A3243G-PEO subject 14504.299
GSM24660A3243G-PEO subject 26162.499
GSM24661A3243G-PEO subject 34519.499
GSM24662A3243G-PEO subject 44904.999
GSM24663mtDNA "Common"-deletion subject 19336.699
GSM24664mtDNA "Common"-deletion subject 212115.399
GSM24665mtDNA "Common"-deletion subject 312134.499
GSM24666mtDNA "Common"-deletion subject 412762.599