ProfileGDS1065 / 215327_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 12% 8% 20% 11% 22% 14% 14% 38% 14% 17% 12% 14% 11% 14% 14% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 14.812
GSM24653Normal subject 23.78
GSM24654Normal subject 39.920
GSM24655A3243G-MELAS subject 13.911
GSM24656A3243G-MELAS subject 211.922
GSM24657A3243G-MELAS subject 37.514
GSM24658A3243G-MELAS subject 44.614
GSM24659A3243G-PEO subject 122.938
GSM24660A3243G-PEO subject 25.914
GSM24661A3243G-PEO subject 35.217
GSM24662A3243G-PEO subject 44.412
GSM24663mtDNA "Common"-deletion subject 16.114
GSM24664mtDNA "Common"-deletion subject 28.211
GSM24665mtDNA "Common"-deletion subject 37.914
GSM24666mtDNA "Common"-deletion subject 47.814