ProfileGDS1065 / 218254_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 94% 93% 95% 95% 93% 94% 94% 95% 93% 95% 92% 93% 96% 94% 95% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1718.194
GSM24653Normal subject 2530.893
GSM24654Normal subject 31291.295
GSM24655A3243G-MELAS subject 1509.595
GSM24656A3243G-MELAS subject 2585.793
GSM24657A3243G-MELAS subject 31116.794
GSM24658A3243G-MELAS subject 4665.594
GSM24659A3243G-PEO subject 155795
GSM24660A3243G-PEO subject 2560.493
GSM24661A3243G-PEO subject 3553.295
GSM24662A3243G-PEO subject 4419.392
GSM24663mtDNA "Common"-deletion subject 1641.293
GSM24664mtDNA "Common"-deletion subject 2187696
GSM24665mtDNA "Common"-deletion subject 31145.494
GSM24666mtDNA "Common"-deletion subject 4148595