ProfileGDS1065 / 200090_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 95% 96% 96% 96% 96% 96% 96% 96% 96% 95% 96% 97% 97% 96% 96% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 11060.795
GSM24653Normal subject 21142.596
GSM24654Normal subject 31419.496
GSM24655A3243G-MELAS subject 1638.296
GSM24656A3243G-MELAS subject 2111996
GSM24657A3243G-MELAS subject 31992.196
GSM24658A3243G-MELAS subject 4973.896
GSM24659A3243G-PEO subject 1779.696
GSM24660A3243G-PEO subject 2931.996
GSM24661A3243G-PEO subject 3568.295
GSM24662A3243G-PEO subject 484996
GSM24663mtDNA "Common"-deletion subject 11527.797
GSM24664mtDNA "Common"-deletion subject 22192.197
GSM24665mtDNA "Common"-deletion subject 31850.296
GSM24666mtDNA "Common"-deletion subject 4228196