ProfileGDS1065 / 211888_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 27% 32% 41% 35% 31% 32% 24% 46% 31% 45% 51% 39% 37% 27% 25% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 114.727
GSM24653Normal subject 219.232
GSM24654Normal subject 334.641
GSM24655A3243G-MELAS subject 117.335
GSM24656A3243G-MELAS subject 220.631
GSM24657A3243G-MELAS subject 327.432
GSM24658A3243G-MELAS subject 410.324
GSM24659A3243G-PEO subject 132.646
GSM24660A3243G-PEO subject 216.931
GSM24661A3243G-PEO subject 325.445
GSM24662A3243G-PEO subject 439.351
GSM24663mtDNA "Common"-deletion subject 127.439
GSM24664mtDNA "Common"-deletion subject 244.837
GSM24665mtDNA "Common"-deletion subject 321.527
GSM24666mtDNA "Common"-deletion subject 418.225