ProfileGDS1065 / 218325_s_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 68% 79% 77% 72% 79% 79% 82% 60% 69% 71% 68% 76% 75% 76% 80% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 196.468
GSM24653Normal subject 2162.579
GSM24654Normal subject 3192.477
GSM24655A3243G-MELAS subject 175.572
GSM24656A3243G-MELAS subject 2168.679
GSM24657A3243G-MELAS subject 3277.779
GSM24658A3243G-MELAS subject 4187.382
GSM24659A3243G-PEO subject 155.260
GSM24660A3243G-PEO subject 287.669
GSM24661A3243G-PEO subject 376.171
GSM24662A3243G-PEO subject 477.768
GSM24663mtDNA "Common"-deletion subject 1152.376
GSM24664mtDNA "Common"-deletion subject 2241.175
GSM24665mtDNA "Common"-deletion subject 322576
GSM24666mtDNA "Common"-deletion subject 4315.780