ProfileGDS1065 / 202298_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 99% 99% 99% 99% 99% 99% 99% 99% 99% 99% 99% 99% 99% 99% 99% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 17947.199
GSM24653Normal subject 28047.799
GSM24654Normal subject 35232.399
GSM24655A3243G-MELAS subject 1315299
GSM24656A3243G-MELAS subject 2550499
GSM24657A3243G-MELAS subject 310098.199
GSM24658A3243G-MELAS subject 4591199
GSM24659A3243G-PEO subject 16069.399
GSM24660A3243G-PEO subject 25915.999
GSM24661A3243G-PEO subject 35593.699
GSM24662A3243G-PEO subject 47820.199
GSM24663mtDNA "Common"-deletion subject 17326.599
GSM24664mtDNA "Common"-deletion subject 28567.299
GSM24665mtDNA "Common"-deletion subject 37957.399
GSM24666mtDNA "Common"-deletion subject 410616.299