ProfileGDS1065 / 217723_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 29% 22% 25% 19% 20% 22% 24% 21% 22% 23% 24% 24% 22% 18% 18% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 116.629
GSM24653Normal subject 210.222
GSM24654Normal subject 314.325
GSM24655A3243G-MELAS subject 16.919
GSM24656A3243G-MELAS subject 210.120
GSM24657A3243G-MELAS subject 314.422
GSM24658A3243G-MELAS subject 410.224
GSM24659A3243G-PEO subject 19.421
GSM24660A3243G-PEO subject 29.922
GSM24661A3243G-PEO subject 37.823
GSM24662A3243G-PEO subject 410.324
GSM24663mtDNA "Common"-deletion subject 111.224
GSM24664mtDNA "Common"-deletion subject 218.922
GSM24665mtDNA "Common"-deletion subject 311.318
GSM24666mtDNA "Common"-deletion subject 410.418