ProfileGDS1065 / 215770_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 31% 6% 18% 29% 35% 17% 22% 23% 31% 29% 15% 28% 31% 24% 18% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 118.731
GSM24653Normal subject 236
GSM24654Normal subject 38.418
GSM24655A3243G-MELAS subject 112.529
GSM24656A3243G-MELAS subject 225.135
GSM24657A3243G-MELAS subject 39.317
GSM24658A3243G-MELAS subject 48.922
GSM24659A3243G-PEO subject 110.723
GSM24660A3243G-PEO subject 217.631
GSM24661A3243G-PEO subject 311.329
GSM24662A3243G-PEO subject 45.315
GSM24663mtDNA "Common"-deletion subject 114.928
GSM24664mtDNA "Common"-deletion subject 233.331
GSM24665mtDNA "Common"-deletion subject 316.824
GSM24666mtDNA "Common"-deletion subject 410.518