ProfileGDS1065 / 205052_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 84% 87% 87% 82% 85% 85% 86% 79% 78% 77% 75% 85% 86% 85% 86% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1244.384
GSM24653Normal subject 227587
GSM24654Normal subject 3402.787
GSM24655A3243G-MELAS subject 1128.182
GSM24656A3243G-MELAS subject 2248.185
GSM24657A3243G-MELAS subject 3405.285
GSM24658A3243G-MELAS subject 4268.986
GSM24659A3243G-PEO subject 1125.579
GSM24660A3243G-PEO subject 213878
GSM24661A3243G-PEO subject 3105.177
GSM24662A3243G-PEO subject 4113.275
GSM24663mtDNA "Common"-deletion subject 1267.585
GSM24664mtDNA "Common"-deletion subject 2500.186
GSM24665mtDNA "Common"-deletion subject 3419.285
GSM24666mtDNA "Common"-deletion subject 4494.786