ProfileGDS1065 / 200031_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% 100% 99% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 111209.899
GSM24653Normal subject 29367.399
GSM24654Normal subject 310730.799
GSM24655A3243G-MELAS subject 1466799
GSM24656A3243G-MELAS subject 27435.299
GSM24657A3243G-MELAS subject 310146.499
GSM24658A3243G-MELAS subject 410121.699
GSM24659A3243G-PEO subject 17392.499
GSM24660A3243G-PEO subject 27491.399
GSM24661A3243G-PEO subject 37753.899
GSM24662A3243G-PEO subject 49114.999
GSM24663mtDNA "Common"-deletion subject 110967.699
GSM24664mtDNA "Common"-deletion subject 212253.999
GSM24665mtDNA "Common"-deletion subject 312902.5100
GSM24666mtDNA "Common"-deletion subject 413724.699