ProfileGDS1065 / 203397_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 15% 21% 10% 12% 25% 9% 18% 6% 4% 27% 11% 22% 29% 12% 8% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 16.415
GSM24653Normal subject 29.321
GSM24654Normal subject 34.410
GSM24655A3243G-MELAS subject 14.312
GSM24656A3243G-MELAS subject 213.825
GSM24657A3243G-MELAS subject 34.89
GSM24658A3243G-MELAS subject 46.418
GSM24659A3243G-PEO subject 13.26
GSM24660A3243G-PEO subject 22.44
GSM24661A3243G-PEO subject 310.127
GSM24662A3243G-PEO subject 43.811
GSM24663mtDNA "Common"-deletion subject 110.122
GSM24664mtDNA "Common"-deletion subject 229.229
GSM24665mtDNA "Common"-deletion subject 37.212
GSM24666mtDNA "Common"-deletion subject 44.78