ProfileGDS1065 / 217559_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 52% 48% 52% 35% 68% 58% 44% 68% 63% 59% 70% 53% 61% 60% 51% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 148.252
GSM24653Normal subject 239.648
GSM24654Normal subject 356.952
GSM24655A3243G-MELAS subject 117.835
GSM24656A3243G-MELAS subject 293.368
GSM24657A3243G-MELAS subject 392.158
GSM24658A3243G-MELAS subject 430.544
GSM24659A3243G-PEO subject 172.368
GSM24660A3243G-PEO subject 269.463
GSM24661A3243G-PEO subject 34659
GSM24662A3243G-PEO subject 484.370
GSM24663mtDNA "Common"-deletion subject 15253
GSM24664mtDNA "Common"-deletion subject 2124.761
GSM24665mtDNA "Common"-deletion subject 399.560
GSM24666mtDNA "Common"-deletion subject 470.851