ProfileGDS1065 / 210632_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 96% 94% 91% 95% 96% 97% 95% 97% 98% 98% 97% 97% 95% 93% 94% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 11374.296
GSM24653Normal subject 2654.494
GSM24654Normal subject 363591
GSM24655A3243G-MELAS subject 156495
GSM24656A3243G-MELAS subject 21192.696
GSM24657A3243G-MELAS subject 3225897
GSM24658A3243G-MELAS subject 4756.895
GSM24659A3243G-PEO subject 11409.797
GSM24660A3243G-PEO subject 21970.298
GSM24661A3243G-PEO subject 31610.598
GSM24662A3243G-PEO subject 41476.597
GSM24663mtDNA "Common"-deletion subject 11844.597
GSM24664mtDNA "Common"-deletion subject 21569.395
GSM24665mtDNA "Common"-deletion subject 31035.593
GSM24666mtDNA "Common"-deletion subject 41355.694