ProfileGDS1065 / 209771_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 67% 44% 41% 46% 30% 61% 66% 57% 63% 59% 54% 59% 48% 54% 51% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 189.567
GSM24653Normal subject 233.244
GSM24654Normal subject 335.541
GSM24655A3243G-MELAS subject 128.246
GSM24656A3243G-MELAS subject 219.330
GSM24657A3243G-MELAS subject 3106.661
GSM24658A3243G-MELAS subject 480.666
GSM24659A3243G-PEO subject 147.657
GSM24660A3243G-PEO subject 267.463
GSM24661A3243G-PEO subject 345.659
GSM24662A3243G-PEO subject 443.554
GSM24663mtDNA "Common"-deletion subject 165.259
GSM24664mtDNA "Common"-deletion subject 274.148
GSM24665mtDNA "Common"-deletion subject 378.154
GSM24666mtDNA "Common"-deletion subject 470.651