ProfileGDS1065 / 203849_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 13% 3% 23% 37% 45% 28% 27% 37% 17% 42% 44% 36% 4% 26% 18% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 15.313
GSM24653Normal subject 21.83
GSM24654Normal subject 312.223
GSM24655A3243G-MELAS subject 118.837
GSM24656A3243G-MELAS subject 239.445
GSM24657A3243G-MELAS subject 321.328
GSM24658A3243G-MELAS subject 412.127
GSM24659A3243G-PEO subject 121.937
GSM24660A3243G-PEO subject 27.217
GSM24661A3243G-PEO subject 322.142
GSM24662A3243G-PEO subject 429.344
GSM24663mtDNA "Common"-deletion subject 123.236
GSM24664mtDNA "Common"-deletion subject 23.84
GSM24665mtDNA "Common"-deletion subject 319.726
GSM24666mtDNA "Common"-deletion subject 410.818