ProfileGDS1065 / 210971_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 1% 1% 18% 3% 0% 3% 3% 8% 4% 9% 1% 10% 14% 2% 0% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 10.71
GSM24653Normal subject 211
GSM24654Normal subject 38.618
GSM24655A3243G-MELAS subject 11.53
GSM24656A3243G-MELAS subject 20.60
GSM24657A3243G-MELAS subject 32.43
GSM24658A3243G-MELAS subject 41.63
GSM24659A3243G-PEO subject 13.68
GSM24660A3243G-PEO subject 22.34
GSM24661A3243G-PEO subject 339
GSM24662A3243G-PEO subject 40.81
GSM24663mtDNA "Common"-deletion subject 14.210
GSM24664mtDNA "Common"-deletion subject 210.414
GSM24665mtDNA "Common"-deletion subject 32.12
GSM24666mtDNA "Common"-deletion subject 40.70