ProfileGDS1065 / 208365_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 41% 30% 44% 32% 47% 24% 36% 29% 46% 27% 18% 31% 39% 42% 33% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 130.341
GSM24653Normal subject 217.430
GSM24654Normal subject 341.344
GSM24655A3243G-MELAS subject 115.232
GSM24656A3243G-MELAS subject 241.847
GSM24657A3243G-MELAS subject 316.324
GSM24658A3243G-MELAS subject 421.636
GSM24659A3243G-PEO subject 114.929
GSM24660A3243G-PEO subject 235.646
GSM24661A3243G-PEO subject 39.827
GSM24662A3243G-PEO subject 46.718
GSM24663mtDNA "Common"-deletion subject 118.331
GSM24664mtDNA "Common"-deletion subject 250.939
GSM24665mtDNA "Common"-deletion subject 347.342
GSM24666mtDNA "Common"-deletion subject 430.333