ProfileGDS1065 / 208504_x_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 17% 13% 11% 6% 5% 14% 14% 8% 15% 9% 11% 11% 13% 8% 8% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 17.317
GSM24653Normal subject 25.313
GSM24654Normal subject 3511
GSM24655A3243G-MELAS subject 12.56
GSM24656A3243G-MELAS subject 23.15
GSM24657A3243G-MELAS subject 37.714
GSM24658A3243G-MELAS subject 44.614
GSM24659A3243G-PEO subject 13.68
GSM24660A3243G-PEO subject 26.215
GSM24661A3243G-PEO subject 32.89
GSM24662A3243G-PEO subject 44.111
GSM24663mtDNA "Common"-deletion subject 14.711
GSM24664mtDNA "Common"-deletion subject 29.913
GSM24665mtDNA "Common"-deletion subject 358
GSM24666mtDNA "Common"-deletion subject 44.48