ProfileGDS1065 / 206012_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 60% 63% 56% 48% 59% 63% 62% 70% 65% 63% 65% 65% 50% 57% 50% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 168.560
GSM24653Normal subject 272.163
GSM24654Normal subject 36856
GSM24655A3243G-MELAS subject 130.248
GSM24656A3243G-MELAS subject 266.859
GSM24657A3243G-MELAS subject 3115.863
GSM24658A3243G-MELAS subject 465.362
GSM24659A3243G-PEO subject 18070
GSM24660A3243G-PEO subject 276.265
GSM24661A3243G-PEO subject 353.963
GSM24662A3243G-PEO subject 469.265
GSM24663mtDNA "Common"-deletion subject 184.365
GSM24664mtDNA "Common"-deletion subject 279.150
GSM24665mtDNA "Common"-deletion subject 386.857
GSM24666mtDNA "Common"-deletion subject 467.350