ProfileGDS1065 / 213877_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 24% 28% 23% 29% 20% 40% 46% 25% 24% 30% 29% 49% 22% 18% 43% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 112.124
GSM24653Normal subject 21528
GSM24654Normal subject 311.823
GSM24655A3243G-MELAS subject 112.329
GSM24656A3243G-MELAS subject 210.120
GSM24657A3243G-MELAS subject 34140
GSM24658A3243G-MELAS subject 433.846
GSM24659A3243G-PEO subject 111.725
GSM24660A3243G-PEO subject 211.324
GSM24661A3243G-PEO subject 311.830
GSM24662A3243G-PEO subject 414.429
GSM24663mtDNA "Common"-deletion subject 144.549
GSM24664mtDNA "Common"-deletion subject 219.222
GSM24665mtDNA "Common"-deletion subject 311.118
GSM24666mtDNA "Common"-deletion subject 449.843