ProfileGDS1065 / 213483_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% 59% 49% 43% 50% 57% 49% 37% 47% 43% 37% 49% 60% 59% 59% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 132.943
GSM24653Normal subject 260.559
GSM24654Normal subject 349.649
GSM24655A3243G-MELAS subject 124.443
GSM24656A3243G-MELAS subject 247.950
GSM24657A3243G-MELAS subject 385.957
GSM24658A3243G-MELAS subject 438.349
GSM24659A3243G-PEO subject 121.837
GSM24660A3243G-PEO subject 236.347
GSM24661A3243G-PEO subject 322.943
GSM24662A3243G-PEO subject 421.837
GSM24663mtDNA "Common"-deletion subject 144.249
GSM24664mtDNA "Common"-deletion subject 2120.360
GSM24665mtDNA "Common"-deletion subject 393.459
GSM24666mtDNA "Common"-deletion subject 498.759