ProfileGDS1065 / 220586_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 19% 20% 6% 16% 1% 25% 2% 12% 20% 1% 1% 18% 13% 14% 21% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 18.319
GSM24653Normal subject 2920
GSM24654Normal subject 33.36
GSM24655A3243G-MELAS subject 15.616
GSM24656A3243G-MELAS subject 21.41
GSM24657A3243G-MELAS subject 317.125
GSM24658A3243G-MELAS subject 41.22
GSM24659A3243G-PEO subject 15.212
GSM24660A3243G-PEO subject 28.920
GSM24661A3243G-PEO subject 30.61
GSM24662A3243G-PEO subject 40.61
GSM24663mtDNA "Common"-deletion subject 17.918
GSM24664mtDNA "Common"-deletion subject 29.613
GSM24665mtDNA "Common"-deletion subject 38.214
GSM24666mtDNA "Common"-deletion subject 413.121