ProfileGDS1065 / 201702_s_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 27% 26% 23% 15% 24% 21% 23% 16% 24% 28% 27% 32% 16% 21% 25% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 114.427
GSM24653Normal subject 213.126
GSM24654Normal subject 31223
GSM24655A3243G-MELAS subject 15.115
GSM24656A3243G-MELAS subject 213.124
GSM24657A3243G-MELAS subject 312.921
GSM24658A3243G-MELAS subject 49.223
GSM24659A3243G-PEO subject 16.716
GSM24660A3243G-PEO subject 211.424
GSM24661A3243G-PEO subject 310.528
GSM24662A3243G-PEO subject 412.427
GSM24663mtDNA "Common"-deletion subject 118.432
GSM24664mtDNA "Common"-deletion subject 212.216
GSM24665mtDNA "Common"-deletion subject 313.921
GSM24666mtDNA "Common"-deletion subject 41825