ProfileGDS1065 / 212966_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 9% 13% 33% 27% 6% 25% 32% 29% 34% 16% 22% 29% 27% 28% 21% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 13.99
GSM24653Normal subject 25.213
GSM24654Normal subject 323.233
GSM24655A3243G-MELAS subject 111.527
GSM24656A3243G-MELAS subject 23.56
GSM24657A3243G-MELAS subject 317.625
GSM24658A3243G-MELAS subject 41732
GSM24659A3243G-PEO subject 115.129
GSM24660A3243G-PEO subject 22134
GSM24661A3243G-PEO subject 35.116
GSM24662A3243G-PEO subject 4922
GSM24663mtDNA "Common"-deletion subject 115.829
GSM24664mtDNA "Common"-deletion subject 227.327
GSM24665mtDNA "Common"-deletion subject 321.828
GSM24666mtDNA "Common"-deletion subject 413.921