ProfileGDS1065 / 203184_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 36% 33% 4% 49% 26% 29% 41% 45% 46% 37% 27% 36% 31% 31% 35% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 123.936
GSM24653Normal subject 220.333
GSM24654Normal subject 32.54
GSM24655A3243G-MELAS subject 130.949
GSM24656A3243G-MELAS subject 214.926
GSM24657A3243G-MELAS subject 322.129
GSM24658A3243G-MELAS subject 426.241
GSM24659A3243G-PEO subject 131.445
GSM24660A3243G-PEO subject 235.746
GSM24661A3243G-PEO subject 317.637
GSM24662A3243G-PEO subject 412.227
GSM24663mtDNA "Common"-deletion subject 124.136
GSM24664mtDNA "Common"-deletion subject 234.231
GSM24665mtDNA "Common"-deletion subject 327.831
GSM24666mtDNA "Common"-deletion subject 433.635