ProfileGDS1065 / 216710_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 18% 32% 63% 52% 41% 61% 36% 59% 53% 32% 33% 27% 37% 60% 6% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 17.618
GSM24653Normal subject 219.132
GSM24654Normal subject 394.263
GSM24655A3243G-MELAS subject 135.252
GSM24656A3243G-MELAS subject 232.441
GSM24657A3243G-MELAS subject 3105.461
GSM24658A3243G-MELAS subject 421.536
GSM24659A3243G-PEO subject 152.559
GSM24660A3243G-PEO subject 246.253
GSM24661A3243G-PEO subject 313.532
GSM24662A3243G-PEO subject 417.433
GSM24663mtDNA "Common"-deletion subject 114.427
GSM24664mtDNA "Common"-deletion subject 24637
GSM24665mtDNA "Common"-deletion subject 310060
GSM24666mtDNA "Common"-deletion subject 43.86