ProfileGDS1065 / 220981_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 59% 48% 17% 22% 29% 20% 23% 46% 32% 18% 47% 55% 24% 29% 38% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 164.359
GSM24653Normal subject 239.648
GSM24654Normal subject 38.317
GSM24655A3243G-MELAS subject 1822
GSM24656A3243G-MELAS subject 218.629
GSM24657A3243G-MELAS subject 311.820
GSM24658A3243G-MELAS subject 49.323
GSM24659A3243G-PEO subject 131.946
GSM24660A3243G-PEO subject 218.332
GSM24661A3243G-PEO subject 35.718
GSM24662A3243G-PEO subject 433.447
GSM24663mtDNA "Common"-deletion subject 154.955
GSM24664mtDNA "Common"-deletion subject 221.824
GSM24665mtDNA "Common"-deletion subject 324.429
GSM24666mtDNA "Common"-deletion subject 438.438