ProfileGDS1065 / 208429_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 51% 59% 51% 52% 60% 59% 59% 62% 56% 64% 61% 60% 60% 57% 58% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 146.151
GSM24653Normal subject 260.359
GSM24654Normal subject 355.651
GSM24655A3243G-MELAS subject 135.552
GSM24656A3243G-MELAS subject 27060
GSM24657A3243G-MELAS subject 396.259
GSM24658A3243G-MELAS subject 457.459
GSM24659A3243G-PEO subject 157.862
GSM24660A3243G-PEO subject 252.756
GSM24661A3243G-PEO subject 354.364
GSM24662A3243G-PEO subject 45961
GSM24663mtDNA "Common"-deletion subject 168.760
GSM24664mtDNA "Common"-deletion subject 2120.160
GSM24665mtDNA "Common"-deletion subject 388.457
GSM24666mtDNA "Common"-deletion subject 494.158