ProfileGDS1065 / 217686_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 6% 6% 7% 5% 6% 4% 11% 9% 7% 6% 6% 11% 8% 5% 7% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 12.86
GSM24653Normal subject 236
GSM24654Normal subject 33.67
GSM24655A3243G-MELAS subject 12.35
GSM24656A3243G-MELAS subject 23.46
GSM24657A3243G-MELAS subject 32.74
GSM24658A3243G-MELAS subject 43.711
GSM24659A3243G-PEO subject 13.99
GSM24660A3243G-PEO subject 23.17
GSM24661A3243G-PEO subject 32.16
GSM24662A3243G-PEO subject 42.66
GSM24663mtDNA "Common"-deletion subject 14.611
GSM24664mtDNA "Common"-deletion subject 26.48
GSM24665mtDNA "Common"-deletion subject 33.55
GSM24666mtDNA "Common"-deletion subject 44.17