ProfileGDS1065 / 823_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 69% 76% 64% 69% 71% 68% 76% 65% 76% 72% 73% 74% 63% 58% 62% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 199.169
GSM24653Normal subject 2133.176
GSM24654Normal subject 399.864
GSM24655A3243G-MELAS subject 166.769
GSM24656A3243G-MELAS subject 2111.671
GSM24657A3243G-MELAS subject 314768
GSM24658A3243G-MELAS subject 4131.376
GSM24659A3243G-PEO subject 165.765
GSM24660A3243G-PEO subject 2121.876
GSM24661A3243G-PEO subject 378.472
GSM24662A3243G-PEO subject 497.773
GSM24663mtDNA "Common"-deletion subject 1133.474
GSM24664mtDNA "Common"-deletion subject 2137.763
GSM24665mtDNA "Common"-deletion subject 389.858
GSM24666mtDNA "Common"-deletion subject 4113.562