ProfileGDS1065 / 221141_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 55% 36% 51% 55% 39% 48% 32% 38% 62% 33% 58% 37% 48% 42% 42% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 155.855
GSM24653Normal subject 223.136
GSM24654Normal subject 355.251
GSM24655A3243G-MELAS subject 138.255
GSM24656A3243G-MELAS subject 230.139
GSM24657A3243G-MELAS subject 357.948
GSM24658A3243G-MELAS subject 416.632
GSM24659A3243G-PEO subject 123.738
GSM24660A3243G-PEO subject 264.562
GSM24661A3243G-PEO subject 313.933
GSM24662A3243G-PEO subject 450.758
GSM24663mtDNA "Common"-deletion subject 124.637
GSM24664mtDNA "Common"-deletion subject 27448
GSM24665mtDNA "Common"-deletion subject 345.842
GSM24666mtDNA "Common"-deletion subject 447.342