ProfileGDS1065 / 214772_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 30% 50% 36% 53% 43% 32% 42% 43% 36% 47% 37% 46% 40% 46% 26% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 11730
GSM24653Normal subject 241.950
GSM24654Normal subject 328.536
GSM24655A3243G-MELAS subject 136.253
GSM24656A3243G-MELAS subject 235.643
GSM24657A3243G-MELAS subject 327.932
GSM24658A3243G-MELAS subject 427.642
GSM24659A3243G-PEO subject 128.943
GSM24660A3243G-PEO subject 222.736
GSM24661A3243G-PEO subject 327.547
GSM24662A3243G-PEO subject 42237
GSM24663mtDNA "Common"-deletion subject 138.346
GSM24664mtDNA "Common"-deletion subject 251.740
GSM24665mtDNA "Common"-deletion subject 354.546
GSM24666mtDNA "Common"-deletion subject 419.826