ProfileGDS1065 / 204586_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 15% 17% 19% 16% 16% 15% 17% 16% 16% 20% 20% 20% 17% 36% 14% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1615
GSM24653Normal subject 2717
GSM24654Normal subject 39.219
GSM24655A3243G-MELAS subject 15.616
GSM24656A3243G-MELAS subject 27.916
GSM24657A3243G-MELAS subject 38.115
GSM24658A3243G-MELAS subject 45.917
GSM24659A3243G-PEO subject 16.816
GSM24660A3243G-PEO subject 26.716
GSM24661A3243G-PEO subject 36.320
GSM24662A3243G-PEO subject 47.520
GSM24663mtDNA "Common"-deletion subject 18.920
GSM24664mtDNA "Common"-deletion subject 213.217
GSM24665mtDNA "Common"-deletion subject 33536
GSM24666mtDNA "Common"-deletion subject 4814