ProfileGDS1065 / 210268_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 20% 35% 36% 7% 9% 8% 36% 20% 21% 23% 18% 27% 21% 28% 35% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 19.320
GSM24653Normal subject 222.335
GSM24654Normal subject 328.636
GSM24655A3243G-MELAS subject 12.77
GSM24656A3243G-MELAS subject 24.59
GSM24657A3243G-MELAS subject 34.68
GSM24658A3243G-MELAS subject 420.936
GSM24659A3243G-PEO subject 18.820
GSM24660A3243G-PEO subject 29.821
GSM24661A3243G-PEO subject 37.823
GSM24662A3243G-PEO subject 46.818
GSM24663mtDNA "Common"-deletion subject 113.727
GSM24664mtDNA "Common"-deletion subject 217.721
GSM24665mtDNA "Common"-deletion subject 322.628
GSM24666mtDNA "Common"-deletion subject 432.535