ProfileGDS1065 / 209223_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 7% 40% 14% 17% 30% 9% 37% 16% 7% 4% 14% 22% 13% 29% 33% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 13.37
GSM24653Normal subject 227.740
GSM24654Normal subject 36.714
GSM24655A3243G-MELAS subject 16.117
GSM24656A3243G-MELAS subject 21930
GSM24657A3243G-MELAS subject 34.99
GSM24658A3243G-MELAS subject 421.737
GSM24659A3243G-PEO subject 16.716
GSM24660A3243G-PEO subject 23.37
GSM24661A3243G-PEO subject 31.84
GSM24662A3243G-PEO subject 45.114
GSM24663mtDNA "Common"-deletion subject 11022
GSM24664mtDNA "Common"-deletion subject 29.813
GSM24665mtDNA "Common"-deletion subject 324.129
GSM24666mtDNA "Common"-deletion subject 429.533