ProfileGDS1065 / 211618_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 7% 4% 5% 3% 3% 6% 3% 10% 11% 9% 5% 11% 5% 10% 25% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 13.37
GSM24653Normal subject 22.34
GSM24654Normal subject 32.95
GSM24655A3243G-MELAS subject 11.73
GSM24656A3243G-MELAS subject 22.13
GSM24657A3243G-MELAS subject 33.46
GSM24658A3243G-MELAS subject 41.43
GSM24659A3243G-PEO subject 14.310
GSM24660A3243G-PEO subject 24.811
GSM24661A3243G-PEO subject 32.89
GSM24662A3243G-PEO subject 42.35
GSM24663mtDNA "Common"-deletion subject 14.511
GSM24664mtDNA "Common"-deletion subject 24.65
GSM24665mtDNA "Common"-deletion subject 35.710
GSM24666mtDNA "Common"-deletion subject 418.625