ProfileGDS1065 / 208764_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 98% 97% 98% 98% 98% 98% 98% 98% 98% 98% 98% 98% 98% 99% 98% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 13245.898
GSM24653Normal subject 21960.497
GSM24654Normal subject 33822.298
GSM24655A3243G-MELAS subject 11221.398
GSM24656A3243G-MELAS subject 22982.698
GSM24657A3243G-MELAS subject 34160.598
GSM24658A3243G-MELAS subject 43691.798
GSM24659A3243G-PEO subject 11702.398
GSM24660A3243G-PEO subject 22904.498
GSM24661A3243G-PEO subject 31555.398
GSM24662A3243G-PEO subject 42057.898
GSM24663mtDNA "Common"-deletion subject 12799.398
GSM24664mtDNA "Common"-deletion subject 24578.498
GSM24665mtDNA "Common"-deletion subject 35962.599
GSM24666mtDNA "Common"-deletion subject 44018.698