ProfileGDS1065 / 220735_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 4% 37% 27% 2% 27% 15% 8% 4% 6% 6% 6% 28% 25% 17% 15% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 12.34
GSM24653Normal subject 224.337
GSM24654Normal subject 316.127
GSM24655A3243G-MELAS subject 11.12
GSM24656A3243G-MELAS subject 215.927
GSM24657A3243G-MELAS subject 38.515
GSM24658A3243G-MELAS subject 42.78
GSM24659A3243G-PEO subject 12.34
GSM24660A3243G-PEO subject 236
GSM24661A3243G-PEO subject 326
GSM24662A3243G-PEO subject 42.66
GSM24663mtDNA "Common"-deletion subject 114.528
GSM24664mtDNA "Common"-deletion subject 223.525
GSM24665mtDNA "Common"-deletion subject 39.917
GSM24666mtDNA "Common"-deletion subject 48.715