ProfileGDS1065 / 201643_x_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 89% 89% 89% 88% 89% 87% 87% 87% 88% 86% 86% 87% 89% 89% 89% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1378.989
GSM24653Normal subject 2339.589
GSM24654Normal subject 3462.589
GSM24655A3243G-MELAS subject 1192.188
GSM24656A3243G-MELAS subject 2365.789
GSM24657A3243G-MELAS subject 3491.587
GSM24658A3243G-MELAS subject 4279.387
GSM24659A3243G-PEO subject 1213.187
GSM24660A3243G-PEO subject 2278.788
GSM24661A3243G-PEO subject 318286
GSM24662A3243G-PEO subject 4219.486
GSM24663mtDNA "Common"-deletion subject 130987
GSM24664mtDNA "Common"-deletion subject 2613.689
GSM24665mtDNA "Common"-deletion subject 3611.689
GSM24666mtDNA "Common"-deletion subject 4693.189