ProfileGDS1065 / 40093_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 81% 86% 69% 84% 78% 87% 78% 87% 83% 87% 83% 84% 71% 65% 74% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1196.281
GSM24653Normal subject 2255.286
GSM24654Normal subject 3126.369
GSM24655A3243G-MELAS subject 1145.184
GSM24656A3243G-MELAS subject 2160.778
GSM24657A3243G-MELAS subject 3488.887
GSM24658A3243G-MELAS subject 4153.678
GSM24659A3243G-PEO subject 1207.987
GSM24660A3243G-PEO subject 2195.283
GSM24661A3243G-PEO subject 3199.387
GSM24662A3243G-PEO subject 4182.183
GSM24663mtDNA "Common"-deletion subject 1243.984
GSM24664mtDNA "Common"-deletion subject 2190.571
GSM24665mtDNA "Common"-deletion subject 3123.965
GSM24666mtDNA "Common"-deletion subject 4208.974