ProfileGDS1065 / 206203_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 28% 35% 35% 42% 38% 32% 49% 28% 35% 40% 24% 45% 23% 32% 21% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 115.428
GSM24653Normal subject 222.435
GSM24654Normal subject 32735
GSM24655A3243G-MELAS subject 124.242
GSM24656A3243G-MELAS subject 228.238
GSM24657A3243G-MELAS subject 327.732
GSM24658A3243G-MELAS subject 437.749
GSM24659A3243G-PEO subject 114.128
GSM24660A3243G-PEO subject 221.935
GSM24661A3243G-PEO subject 320.640
GSM24662A3243G-PEO subject 410.424
GSM24663mtDNA "Common"-deletion subject 13745
GSM24664mtDNA "Common"-deletion subject 220.423
GSM24665mtDNA "Common"-deletion subject 329.232
GSM24666mtDNA "Common"-deletion subject 413.221