ProfileGDS1065 / 222270_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 24% 49% 40% 37% 37% 45% 36% 12% 30% 47% 38% 28% 35% 38% 41% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 112.124
GSM24653Normal subject 24149
GSM24654Normal subject 333.440
GSM24655A3243G-MELAS subject 118.837
GSM24656A3243G-MELAS subject 227.537
GSM24657A3243G-MELAS subject 352.245
GSM24658A3243G-MELAS subject 421.436
GSM24659A3243G-PEO subject 14.912
GSM24660A3243G-PEO subject 216.830
GSM24661A3243G-PEO subject 327.847
GSM24662A3243G-PEO subject 42338
GSM24663mtDNA "Common"-deletion subject 114.928
GSM24664mtDNA "Common"-deletion subject 241.135
GSM24665mtDNA "Common"-deletion subject 339.338
GSM24666mtDNA "Common"-deletion subject 444.941