ProfileGDS1065 / 213580_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 7% 21% 1% 18% 8% 6% 2% 28% 17% 2% 1% 1% 18% 16% 21% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 13.27
GSM24653Normal subject 29.321
GSM24654Normal subject 31.11
GSM24655A3243G-MELAS subject 16.218
GSM24656A3243G-MELAS subject 24.38
GSM24657A3243G-MELAS subject 33.56
GSM24658A3243G-MELAS subject 41.12
GSM24659A3243G-PEO subject 113.928
GSM24660A3243G-PEO subject 27.117
GSM24661A3243G-PEO subject 31.22
GSM24662A3243G-PEO subject 40.81
GSM24663mtDNA "Common"-deletion subject 10.71
GSM24664mtDNA "Common"-deletion subject 214.218
GSM24665mtDNA "Common"-deletion subject 39.516
GSM24666mtDNA "Common"-deletion subject 413.821