ProfileGDS1065 / 218016_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 89% 90% 91% 87% 87% 87% 87% 83% 87% 85% 83% 88% 90% 91% 87% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 137989
GSM24653Normal subject 2386.390
GSM24654Normal subject 3591.191
GSM24655A3243G-MELAS subject 1179.387
GSM24656A3243G-MELAS subject 2295.387
GSM24657A3243G-MELAS subject 3510.887
GSM24658A3243G-MELAS subject 4291.587
GSM24659A3243G-PEO subject 1156.883
GSM24660A3243G-PEO subject 2265.487
GSM24661A3243G-PEO subject 3166.185
GSM24662A3243G-PEO subject 4180.583
GSM24663mtDNA "Common"-deletion subject 1358.588
GSM24664mtDNA "Common"-deletion subject 2700.990
GSM24665mtDNA "Common"-deletion subject 3747.791
GSM24666mtDNA "Common"-deletion subject 4538.587