ProfileGDS1065 / 201551_s_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 37% 50% 64% 59% 53% 40% 42% 46% 46% 32% 34% 29% 51% 59% 53% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 125.337
GSM24653Normal subject 243.350
GSM24654Normal subject 397.764
GSM24655A3243G-MELAS subject 144.759
GSM24656A3243G-MELAS subject 25253
GSM24657A3243G-MELAS subject 341.440
GSM24658A3243G-MELAS subject 428.542
GSM24659A3243G-PEO subject 133.146
GSM24660A3243G-PEO subject 235.546
GSM24661A3243G-PEO subject 313.732
GSM24662A3243G-PEO subject 41934
GSM24663mtDNA "Common"-deletion subject 11629
GSM24664mtDNA "Common"-deletion subject 28351
GSM24665mtDNA "Common"-deletion subject 395.259
GSM24666mtDNA "Common"-deletion subject 476.453