ProfileGDS1065 / 201694_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 71% 74% 57% 85% 82% 84% 87% 85% 60% 72% 78% 70% 85% 68% 65% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1111.771
GSM24653Normal subject 211974
GSM24654Normal subject 373.257
GSM24655A3243G-MELAS subject 1151.585
GSM24656A3243G-MELAS subject 2195.482
GSM24657A3243G-MELAS subject 3388.484
GSM24658A3243G-MELAS subject 4285.287
GSM24659A3243G-PEO subject 1175.985
GSM24660A3243G-PEO subject 260.360
GSM24661A3243G-PEO subject 379.372
GSM24662A3243G-PEO subject 4132.778
GSM24663mtDNA "Common"-deletion subject 1110.370
GSM24664mtDNA "Common"-deletion subject 2439.585
GSM24665mtDNA "Common"-deletion subject 3138.868
GSM24666mtDNA "Common"-deletion subject 4131.765