ProfileGDS1065 / 218203_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 86% 87% 87% 85% 85% 87% 85% 87% 86% 88% 87% 88% 89% 88% 88% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1292.786
GSM24653Normal subject 2292.987
GSM24654Normal subject 3386.287
GSM24655A3243G-MELAS subject 1157.685
GSM24656A3243G-MELAS subject 2253.385
GSM24657A3243G-MELAS subject 3482.287
GSM24658A3243G-MELAS subject 423685
GSM24659A3243G-PEO subject 1199.787
GSM24660A3243G-PEO subject 2235.986
GSM24661A3243G-PEO subject 3213.688
GSM24662A3243G-PEO subject 4244.987
GSM24663mtDNA "Common"-deletion subject 1356.588
GSM24664mtDNA "Common"-deletion subject 2617.289
GSM24665mtDNA "Common"-deletion subject 3534.388
GSM24666mtDNA "Common"-deletion subject 4572.888