ProfileGDS1065 / 221045_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 83% 66% 80% 76% 82% 84% 80% 78% 80% 84% 78% 82% 78% 84% 86% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1224.483
GSM24653Normal subject 280.866
GSM24654Normal subject 3229.880
GSM24655A3243G-MELAS subject 191.476
GSM24656A3243G-MELAS subject 2199.682
GSM24657A3243G-MELAS subject 3391.684
GSM24658A3243G-MELAS subject 4175.280
GSM24659A3243G-PEO subject 1115.178
GSM24660A3243G-PEO subject 2156.480
GSM24661A3243G-PEO subject 3161.284
GSM24662A3243G-PEO subject 4127.478
GSM24663mtDNA "Common"-deletion subject 1220.482
GSM24664mtDNA "Common"-deletion subject 2286.878
GSM24665mtDNA "Common"-deletion subject 3370.684
GSM24666mtDNA "Common"-deletion subject 4517.886