ProfileGDS1065 / 207380_x_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 43% 30% 27% 21% 21% 30% 21% 53% 34% 23% 63% 48% 22% 25% 15% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 132.843
GSM24653Normal subject 216.830
GSM24654Normal subject 316.227
GSM24655A3243G-MELAS subject 17.821
GSM24656A3243G-MELAS subject 211.221
GSM24657A3243G-MELAS subject 323.930
GSM24658A3243G-MELAS subject 48.421
GSM24659A3243G-PEO subject 141.253
GSM24660A3243G-PEO subject 221.134
GSM24661A3243G-PEO subject 37.523
GSM24662A3243G-PEO subject 464.563
GSM24663mtDNA "Common"-deletion subject 141.148
GSM24664mtDNA "Common"-deletion subject 218.322
GSM24665mtDNA "Common"-deletion subject 318.825
GSM24666mtDNA "Common"-deletion subject 48.715