ProfileGDS1065 / 221212_x_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% 16% 5% 18% 17% 7% 20% 17% 12% 6% 28% 19% 18% 12% 23% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 16.215
GSM24653Normal subject 26.416
GSM24654Normal subject 32.75
GSM24655A3243G-MELAS subject 16.418
GSM24656A3243G-MELAS subject 28.517
GSM24657A3243G-MELAS subject 347
GSM24658A3243G-MELAS subject 47.220
GSM24659A3243G-PEO subject 17.217
GSM24660A3243G-PEO subject 25.112
GSM24661A3243G-PEO subject 32.26
GSM24662A3243G-PEO subject 413.128
GSM24663mtDNA "Common"-deletion subject 18.419
GSM24664mtDNA "Common"-deletion subject 213.718
GSM24665mtDNA "Common"-deletion subject 37.212
GSM24666mtDNA "Common"-deletion subject 41623