ProfileGDS1065 / 211930_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 63% 57% 67% 35% 52% 56% 60% 38% 56% 48% 46% 48% 57% 66% 60% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 177.763
GSM24653Normal subject 256.457
GSM24654Normal subject 3114.867
GSM24655A3243G-MELAS subject 117.135
GSM24656A3243G-MELAS subject 250.952
GSM24657A3243G-MELAS subject 384.456
GSM24658A3243G-MELAS subject 46060
GSM24659A3243G-PEO subject 123.338
GSM24660A3243G-PEO subject 251.956
GSM24661A3243G-PEO subject 328.948
GSM24662A3243G-PEO subject 432.546
GSM24663mtDNA "Common"-deletion subject 142.148
GSM24664mtDNA "Common"-deletion subject 2102.457
GSM24665mtDNA "Common"-deletion subject 3129.566
GSM24666mtDNA "Common"-deletion subject 4105.860