ProfileGDS1065 / 206353_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 16545.799
GSM24653Normal subject 24227.999
GSM24654Normal subject 38386.999
GSM24655A3243G-MELAS subject 1342499
GSM24656A3243G-MELAS subject 26457.899
GSM24657A3243G-MELAS subject 38380.699
GSM24658A3243G-MELAS subject 44297.299
GSM24659A3243G-PEO subject 15221.499
GSM24660A3243G-PEO subject 26706.599
GSM24661A3243G-PEO subject 34777.799
GSM24662A3243G-PEO subject 45589.399
GSM24663mtDNA "Common"-deletion subject 15166.499
GSM24664mtDNA "Common"-deletion subject 27812.799
GSM24665mtDNA "Common"-deletion subject 39459.299
GSM24666mtDNA "Common"-deletion subject 4868599