ProfileGDS1065 / 208996_s_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 82% 81% 86% 84% 85% 82% 84% 86% 83% 73% 78% 81% 87% 87% 82% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1210.982
GSM24653Normal subject 2186.281
GSM24654Normal subject 336786
GSM24655A3243G-MELAS subject 1148.784
GSM24656A3243G-MELAS subject 2257.785
GSM24657A3243G-MELAS subject 3340.282
GSM24658A3243G-MELAS subject 4225.384
GSM24659A3243G-PEO subject 1189.586
GSM24660A3243G-PEO subject 2198.783
GSM24661A3243G-PEO subject 383.273
GSM24662A3243G-PEO subject 4133.778
GSM24663mtDNA "Common"-deletion subject 1204.781
GSM24664mtDNA "Common"-deletion subject 2534.187
GSM24665mtDNA "Common"-deletion subject 3467.187
GSM24666mtDNA "Common"-deletion subject 4359.182