ProfileGDS1065 / 201216_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 77% 83% 81% 88% 83% 86% 89% 86% 84% 85% 85% 76% 83% 77% 78% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1158.777
GSM24653Normal subject 221583
GSM24654Normal subject 325281
GSM24655A3243G-MELAS subject 1206.988
GSM24656A3243G-MELAS subject 2217.783
GSM24657A3243G-MELAS subject 3468.886
GSM24658A3243G-MELAS subject 4356.789
GSM24659A3243G-PEO subject 1188.186
GSM24660A3243G-PEO subject 2210.184
GSM24661A3243G-PEO subject 3173.785
GSM24662A3243G-PEO subject 4212.185
GSM24663mtDNA "Common"-deletion subject 1150.476
GSM24664mtDNA "Common"-deletion subject 2388.883
GSM24665mtDNA "Common"-deletion subject 3236.577
GSM24666mtDNA "Common"-deletion subject 4270.878