ProfileGDS1065 / 208176_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 23% 21% 19% 15% 16% 20% 15% 12% 25% 21% 28% 25% 20% 10% 15% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 110.723
GSM24653Normal subject 29.221
GSM24654Normal subject 39.319
GSM24655A3243G-MELAS subject 15.315
GSM24656A3243G-MELAS subject 27.816
GSM24657A3243G-MELAS subject 312.120
GSM24658A3243G-MELAS subject 45.115
GSM24659A3243G-PEO subject 15.112
GSM24660A3243G-PEO subject 212.725
GSM24661A3243G-PEO subject 36.821
GSM24662A3243G-PEO subject 413.228
GSM24663mtDNA "Common"-deletion subject 112.525
GSM24664mtDNA "Common"-deletion subject 216.520
GSM24665mtDNA "Common"-deletion subject 35.810
GSM24666mtDNA "Common"-deletion subject 48.515