ProfileGDS1065 / 200092_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 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 17497.699
GSM24653Normal subject 26184.899
GSM24654Normal subject 36962.199
GSM24655A3243G-MELAS subject 13582.499
GSM24656A3243G-MELAS subject 25201.199
GSM24657A3243G-MELAS subject 39102.999
GSM24658A3243G-MELAS subject 46327.699
GSM24659A3243G-PEO subject 15434.299
GSM24660A3243G-PEO subject 25649.199
GSM24661A3243G-PEO subject 35250.199
GSM24662A3243G-PEO subject 46375.599
GSM24663mtDNA "Common"-deletion subject 1836099
GSM24664mtDNA "Common"-deletion subject 2926899
GSM24665mtDNA "Common"-deletion subject 38364.999
GSM24666mtDNA "Common"-deletion subject 49921.499