ProfileGDS1065 / 37577_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 29% 37% 29% 25% 27% 35% 29% 22% 24% 7% 15% 24% 30% 23% 32% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 115.929
GSM24653Normal subject 224.237
GSM24654Normal subject 318.229
GSM24655A3243G-MELAS subject 19.925
GSM24656A3243G-MELAS subject 216.227
GSM24657A3243G-MELAS subject 332.135
GSM24658A3243G-MELAS subject 413.929
GSM24659A3243G-PEO subject 11022
GSM24660A3243G-PEO subject 211.424
GSM24661A3243G-PEO subject 32.57
GSM24662A3243G-PEO subject 45.315
GSM24663mtDNA "Common"-deletion subject 111.624
GSM24664mtDNA "Common"-deletion subject 232.630
GSM24665mtDNA "Common"-deletion subject 315.923
GSM24666mtDNA "Common"-deletion subject 428.232