ProfileGDS1065 / 205464_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 35% 24% 31% 24% 52% 41% 39% 19% 40% 39% 30% 24% 23% 42% 31% sort by genotype/variation sort by disease state Gene Expression Profile
Graph caption help
SampleTitleValueRank
GSM24652Normal subject 122.635
GSM24653Normal subject 211.224
GSM24654Normal subject 320.631
GSM24655A3243G-MELAS subject 19.124
GSM24656A3243G-MELAS subject 250.452
GSM24657A3243G-MELAS subject 343.341
GSM24658A3243G-MELAS subject 423.939
GSM24659A3243G-PEO subject 1819
GSM24660A3243G-PEO subject 227.240
GSM24661A3243G-PEO subject 319.539
GSM24662A3243G-PEO subject 415.130
GSM24663mtDNA "Common"-deletion subject 111.524
GSM24664mtDNA "Common"-deletion subject 220.623
GSM24665mtDNA "Common"-deletion subject 346.842
GSM24666mtDNA "Common"-deletion subject 426.631