ProfileGDS1065 / 205167_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 35% 35% 33% 34% 34% 24% 28% 24% 27% 44% 21% 26% 30% 24% 25% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 122.235
GSM24653Normal subject 221.835
GSM24654Normal subject 324.433
GSM24655A3243G-MELAS subject 116.834
GSM24656A3243G-MELAS subject 223.834
GSM24657A3243G-MELAS subject 316.524
GSM24658A3243G-MELAS subject 413.328
GSM24659A3243G-PEO subject 111.424
GSM24660A3243G-PEO subject 214.227
GSM24661A3243G-PEO subject 324.344
GSM24662A3243G-PEO subject 47.921
GSM24663mtDNA "Common"-deletion subject 112.826
GSM24664mtDNA "Common"-deletion subject 231.530
GSM24665mtDNA "Common"-deletion subject 316.524
GSM24666mtDNA "Common"-deletion subject 418.825