ProfileGDS1065 / 211771_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 28% 47% 21% 10% 11% 20% 19% 18% 29% 20% 16% 24% 19% 22% 21% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 114.928
GSM24653Normal subject 237.747
GSM24654Normal subject 310.621
GSM24655A3243G-MELAS subject 13.610
GSM24656A3243G-MELAS subject 25.211
GSM24657A3243G-MELAS subject 312.120
GSM24658A3243G-MELAS subject 4719
GSM24659A3243G-PEO subject 17.418
GSM24660A3243G-PEO subject 215.629
GSM24661A3243G-PEO subject 36.320
GSM24662A3243G-PEO subject 45.716
GSM24663mtDNA "Common"-deletion subject 111.124
GSM24664mtDNA "Common"-deletion subject 215.719
GSM24665mtDNA "Common"-deletion subject 315.222
GSM24666mtDNA "Common"-deletion subject 413.921