ProfileGDS1065 / 201907_x_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 18% 12% 13% 17% 19% 16% 10% 54% 13% 23% 14% 15% 15% 15% 8% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 17.818
GSM24653Normal subject 24.812
GSM24654Normal subject 36.113
GSM24655A3243G-MELAS subject 15.817
GSM24656A3243G-MELAS subject 29.419
GSM24657A3243G-MELAS subject 38.916
GSM24658A3243G-MELAS subject 43.210
GSM24659A3243G-PEO subject 143.654
GSM24660A3243G-PEO subject 25.513
GSM24661A3243G-PEO subject 37.823
GSM24662A3243G-PEO subject 44.814
GSM24663mtDNA "Common"-deletion subject 16.215
GSM24664mtDNA "Common"-deletion subject 211.515
GSM24665mtDNA "Common"-deletion subject 38.715
GSM24666mtDNA "Common"-deletion subject 44.38