ProfileGDS1065 / 206859_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 15% 15% 5% 12% 14% 7% 11% 33% 21% 4% 18% 12% 13% 9% 13% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 16.315
GSM24653Normal subject 25.815
GSM24654Normal subject 32.85
GSM24655A3243G-MELAS subject 14.312
GSM24656A3243G-MELAS subject 26.514
GSM24657A3243G-MELAS subject 33.97
GSM24658A3243G-MELAS subject 43.611
GSM24659A3243G-PEO subject 118.333
GSM24660A3243G-PEO subject 29.821
GSM24661A3243G-PEO subject 31.64
GSM24662A3243G-PEO subject 46.518
GSM24663mtDNA "Common"-deletion subject 14.912
GSM24664mtDNA "Common"-deletion subject 29.713
GSM24665mtDNA "Common"-deletion subject 35.69
GSM24666mtDNA "Common"-deletion subject 47.313