ProfileGDS1065 / 218850_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 67% 67% 61% 72% 63% 55% 66% 70% 74% 70% 67% 62% 57% 61% 60% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 191.267
GSM24653Normal subject 284.367
GSM24654Normal subject 385.361
GSM24655A3243G-MELAS subject 176.372
GSM24656A3243G-MELAS subject 277.663
GSM24657A3243G-MELAS subject 38055
GSM24658A3243G-MELAS subject 478.466
GSM24659A3243G-PEO subject 181.670
GSM24660A3243G-PEO subject 2109.574
GSM24661A3243G-PEO subject 372.270
GSM24662A3243G-PEO subject 475.767
GSM24663mtDNA "Common"-deletion subject 177.262
GSM24664mtDNA "Common"-deletion subject 2102.857
GSM24665mtDNA "Common"-deletion subject 3102.861
GSM24666mtDNA "Common"-deletion subject 4102.660