ProfileGDS1065 / 209275_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 64% 45% 54% 51% 53% 55% 66% 51% 40% 33% 59% 66% 51% 63% 39% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 180.364
GSM24653Normal subject 235.445
GSM24654Normal subject 363.954
GSM24655A3243G-MELAS subject 133.251
GSM24656A3243G-MELAS subject 253.253
GSM24657A3243G-MELAS subject 379.655
GSM24658A3243G-MELAS subject 48066
GSM24659A3243G-PEO subject 139.251
GSM24660A3243G-PEO subject 227.940
GSM24661A3243G-PEO subject 31433
GSM24662A3243G-PEO subject 453.559
GSM24663mtDNA "Common"-deletion subject 189.666
GSM24664mtDNA "Common"-deletion subject 280.951
GSM24665mtDNA "Common"-deletion subject 3112.863
GSM24666mtDNA "Common"-deletion subject 441.439