ProfileGDS1065 / 214870_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 80% 91% 87% 48% 77% 89% 87% 39% 44% 56% 45% 83% 88% 90% 88% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1184.180
GSM24653Normal subject 2417.791
GSM24654Normal subject 3406.487
GSM24655A3243G-MELAS subject 130.648
GSM24656A3243G-MELAS subject 2148.977
GSM24657A3243G-MELAS subject 3589.789
GSM24658A3243G-MELAS subject 4282.787
GSM24659A3243G-PEO subject 124.639
GSM24660A3243G-PEO subject 232.144
GSM24661A3243G-PEO subject 340.756
GSM24662A3243G-PEO subject 430.245
GSM24663mtDNA "Common"-deletion subject 1230.783
GSM24664mtDNA "Common"-deletion subject 2560.988
GSM24665mtDNA "Common"-deletion subject 3698.790
GSM24666mtDNA "Common"-deletion subject 4579.688