ProfileGDS1065 / 208129_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 19% 42% 40% 32% 34% 34% 12% 34% 15% 39% 34% 52% 39% 39% 11% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 18.719
GSM24653Normal subject 230.842
GSM24654Normal subject 33340
GSM24655A3243G-MELAS subject 114.932
GSM24656A3243G-MELAS subject 223.734
GSM24657A3243G-MELAS subject 330.934
GSM24658A3243G-MELAS subject 44.212
GSM24659A3243G-PEO subject 11934
GSM24660A3243G-PEO subject 26.615
GSM24661A3243G-PEO subject 319.439
GSM24662A3243G-PEO subject 418.534
GSM24663mtDNA "Common"-deletion subject 148.552
GSM24664mtDNA "Common"-deletion subject 25139
GSM24665mtDNA "Common"-deletion subject 340.439
GSM24666mtDNA "Common"-deletion subject 46.211