ProfileGDS1065 / 213605_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 57% 49% 32% 34% 45% 47% 59% 33% 45% 27% 32% 45% 44% 44% 55% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 159.157
GSM24653Normal subject 241.549
GSM24654Normal subject 321.732
GSM24655A3243G-MELAS subject 116.734
GSM24656A3243G-MELAS subject 238.945
GSM24657A3243G-MELAS subject 357.147
GSM24658A3243G-MELAS subject 458.359
GSM24659A3243G-PEO subject 118.833
GSM24660A3243G-PEO subject 233.945
GSM24661A3243G-PEO subject 39.627
GSM24662A3243G-PEO subject 417.132
GSM24663mtDNA "Common"-deletion subject 13745
GSM24664mtDNA "Common"-deletion subject 260.644
GSM24665mtDNA "Common"-deletion subject 350.444
GSM24666mtDNA "Common"-deletion subject 481.955