ProfileGDS1065 / 209559_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 19% 10% 11% 25% 31% 22% 12% 14% 6% 17% 26% 6% 23% 9% 12% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 18.719
GSM24653Normal subject 24.310
GSM24654Normal subject 35.111
GSM24655A3243G-MELAS subject 19.825
GSM24656A3243G-MELAS subject 220.231
GSM24657A3243G-MELAS subject 313.422
GSM24658A3243G-MELAS subject 44.212
GSM24659A3243G-PEO subject 16.114
GSM24660A3243G-PEO subject 22.96
GSM24661A3243G-PEO subject 35.217
GSM24662A3243G-PEO subject 411.626
GSM24663mtDNA "Common"-deletion subject 136
GSM24664mtDNA "Common"-deletion subject 220.623
GSM24665mtDNA "Common"-deletion subject 35.29
GSM24666mtDNA "Common"-deletion subject 46.512