ProfileGDS1065 / 221591_s_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 42% 31% 25% 50% 30% 53% 22% 38% 23% 36% 23% 26% 38% 31% 21% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 131.942
GSM24653Normal subject 217.931
GSM24654Normal subject 314.125
GSM24655A3243G-MELAS subject 132.450
GSM24656A3243G-MELAS subject 21930
GSM24657A3243G-MELAS subject 374.453
GSM24658A3243G-MELAS subject 4922
GSM24659A3243G-PEO subject 122.938
GSM24660A3243G-PEO subject 210.623
GSM24661A3243G-PEO subject 316.936
GSM24662A3243G-PEO subject 49.223
GSM24663mtDNA "Common"-deletion subject 112.726
GSM24664mtDNA "Common"-deletion subject 248.338
GSM24665mtDNA "Common"-deletion subject 327.131
GSM24666mtDNA "Common"-deletion subject 413.221