ProfileGDS1065 / 210601_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 31% 25% 39% 39% 50% 32% 43% 25% 45% 31% 26% 27% 30% 25% 23% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 118.931
GSM24653Normal subject 212.225
GSM24654Normal subject 332.239
GSM24655A3243G-MELAS subject 121.339
GSM24656A3243G-MELAS subject 247.650
GSM24657A3243G-MELAS subject 327.932
GSM24658A3243G-MELAS subject 429.843
GSM24659A3243G-PEO subject 11225
GSM24660A3243G-PEO subject 233.445
GSM24661A3243G-PEO subject 312.631
GSM24662A3243G-PEO subject 411.826
GSM24663mtDNA "Common"-deletion subject 114.127
GSM24664mtDNA "Common"-deletion subject 232.330
GSM24665mtDNA "Common"-deletion subject 318.425
GSM24666mtDNA "Common"-deletion subject 415.323