ProfileGDS1065 / 222374_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 26% 13% 11% 9% 9% 14% 12% 12% 8% 19% 16% 22% 11% 7% 9% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 113.926
GSM24653Normal subject 25.413
GSM24654Normal subject 35.111
GSM24655A3243G-MELAS subject 13.29
GSM24656A3243G-MELAS subject 24.79
GSM24657A3243G-MELAS subject 37.814
GSM24658A3243G-MELAS subject 4412
GSM24659A3243G-PEO subject 1512
GSM24660A3243G-PEO subject 23.58
GSM24661A3243G-PEO subject 35.819
GSM24662A3243G-PEO subject 46.116
GSM24663mtDNA "Common"-deletion subject 11022
GSM24664mtDNA "Common"-deletion subject 2811
GSM24665mtDNA "Common"-deletion subject 34.77
GSM24666mtDNA "Common"-deletion subject 459