ProfileGDS1065 / 211017_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 11% 6% 16% 7% 4% 23% 22% 7% 9% 7% 3% 9% 6% 3% 25% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 14.411
GSM24653Normal subject 22.96
GSM24654Normal subject 37.516
GSM24655A3243G-MELAS subject 12.97
GSM24656A3243G-MELAS subject 22.84
GSM24657A3243G-MELAS subject 315.123
GSM24658A3243G-MELAS subject 48.822
GSM24659A3243G-PEO subject 13.57
GSM24660A3243G-PEO subject 23.89
GSM24661A3243G-PEO subject 32.57
GSM24662A3243G-PEO subject 41.53
GSM24663mtDNA "Common"-deletion subject 13.89
GSM24664mtDNA "Common"-deletion subject 25.26
GSM24665mtDNA "Common"-deletion subject 32.63
GSM24666mtDNA "Common"-deletion subject 418.625