ProfileGDS1065 / 218324_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 40% 47% 46% 49% 48% 36% 40% 41% 27% 38% 34% 47% 48% 45% 41% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 128.740
GSM24653Normal subject 237.447
GSM24654Normal subject 344.946
GSM24655A3243G-MELAS subject 131.849
GSM24656A3243G-MELAS subject 24448
GSM24657A3243G-MELAS subject 333.636
GSM24658A3243G-MELAS subject 425.440
GSM24659A3243G-PEO subject 126.341
GSM24660A3243G-PEO subject 21427
GSM24661A3243G-PEO subject 318.638
GSM24662A3243G-PEO subject 41934
GSM24663mtDNA "Common"-deletion subject 140.447
GSM24664mtDNA "Common"-deletion subject 273.248
GSM24665mtDNA "Common"-deletion subject 352.145
GSM24666mtDNA "Common"-deletion subject 445.241