ProfileGDS1065 / 207283_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 75% 80% 71% 63% 80% 81% 83% 84% 86% 85% 84% 85% 77% 69% 80% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1135.775
GSM24653Normal subject 2166.180
GSM24654Normal subject 3141.471
GSM24655A3243G-MELAS subject 151.663
GSM24656A3243G-MELAS subject 2178.880
GSM24657A3243G-MELAS subject 3311.781
GSM24658A3243G-MELAS subject 4213.183
GSM24659A3243G-PEO subject 1172.184
GSM24660A3243G-PEO subject 2234.586
GSM24661A3243G-PEO subject 3170.485
GSM24662A3243G-PEO subject 4200.384
GSM24663mtDNA "Common"-deletion subject 1272.285
GSM24664mtDNA "Common"-deletion subject 2264.977
GSM24665mtDNA "Common"-deletion subject 3147.869
GSM24666mtDNA "Common"-deletion subject 430780