ProfileGDS1065 / 212948_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 78% 82% 81% 85% 78% 74% 77% 82% 78% 87% 88% 87% 76% 79% 76% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1168.678
GSM24653Normal subject 218982
GSM24654Normal subject 324181
GSM24655A3243G-MELAS subject 1150.185
GSM24656A3243G-MELAS subject 2157.178
GSM24657A3243G-MELAS subject 3204.674
GSM24658A3243G-MELAS subject 4139.177
GSM24659A3243G-PEO subject 1147.982
GSM24660A3243G-PEO subject 213778
GSM24661A3243G-PEO subject 3203.987
GSM24662A3243G-PEO subject 4257.388
GSM24663mtDNA "Common"-deletion subject 1319.487
GSM24664mtDNA "Common"-deletion subject 2256.276
GSM24665mtDNA "Common"-deletion subject 3257.479
GSM24666mtDNA "Common"-deletion subject 4235.576