ProfileGDS1065 / 216332_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 20% 25% 44% 35% 42% 16% 29% 23% 47% 28% 28% 25% 26% 42% 21% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1920
GSM24653Normal subject 212.325
GSM24654Normal subject 339.944
GSM24655A3243G-MELAS subject 117.735
GSM24656A3243G-MELAS subject 234.642
GSM24657A3243G-MELAS subject 38.916
GSM24658A3243G-MELAS subject 413.629
GSM24659A3243G-PEO subject 110.323
GSM24660A3243G-PEO subject 236.747
GSM24661A3243G-PEO subject 310.228
GSM24662A3243G-PEO subject 412.828
GSM24663mtDNA "Common"-deletion subject 112.525
GSM24664mtDNA "Common"-deletion subject 225.426
GSM24665mtDNA "Common"-deletion subject 347.142
GSM24666mtDNA "Common"-deletion subject 413.621