ProfileGDS1065 / 215411_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% 29% 33% 28% 29% 28% 40% 17% 24% 20% 34% 33% 27% 32% 27% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 114.827
GSM24653Normal subject 216.229
GSM24654Normal subject 32433
GSM24655A3243G-MELAS subject 111.728
GSM24656A3243G-MELAS subject 218.129
GSM24657A3243G-MELAS subject 321.428
GSM24658A3243G-MELAS subject 425.440
GSM24659A3243G-PEO subject 17.117
GSM24660A3243G-PEO subject 211.324
GSM24661A3243G-PEO subject 36.320
GSM24662A3243G-PEO subject 419.334
GSM24663mtDNA "Common"-deletion subject 119.933
GSM24664mtDNA "Common"-deletion subject 226.327
GSM24665mtDNA "Common"-deletion subject 329.332
GSM24666mtDNA "Common"-deletion subject 420.727