ProfileGDS1065 / 221858_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 59% 53% 56% 62% 60% 61% 59% 58% 53% 59% 60% 49% 60% 60% 67% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 163.159
GSM24653Normal subject 247.453
GSM24654Normal subject 368.156
GSM24655A3243G-MELAS subject 150.562
GSM24656A3243G-MELAS subject 268.560
GSM24657A3243G-MELAS subject 3107.361
GSM24658A3243G-MELAS subject 457.959
GSM24659A3243G-PEO subject 150.758
GSM24660A3243G-PEO subject 246.853
GSM24661A3243G-PEO subject 345.159
GSM24662A3243G-PEO subject 45760
GSM24663mtDNA "Common"-deletion subject 143.749
GSM24664mtDNA "Common"-deletion subject 2116.960
GSM24665mtDNA "Common"-deletion subject 397.960
GSM24666mtDNA "Common"-deletion subject 4151.167