ProfileGDS1065 / 201767_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 77% 73% 74% 54% 59% 78% 79% 70% 68% 74% 69% 80% 75% 77% 76% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1151.477
GSM24653Normal subject 2113.773
GSM24654Normal subject 3157.874
GSM24655A3243G-MELAS subject 137.254
GSM24656A3243G-MELAS subject 267.559
GSM24657A3243G-MELAS subject 3260.478
GSM24658A3243G-MELAS subject 4160.979
GSM24659A3243G-PEO subject 181.570
GSM24660A3243G-PEO subject 283.168
GSM24661A3243G-PEO subject 387.874
GSM24662A3243G-PEO subject 482.369
GSM24663mtDNA "Common"-deletion subject 1191.580
GSM24664mtDNA "Common"-deletion subject 2239.775
GSM24665mtDNA "Common"-deletion subject 3230.877
GSM24666mtDNA "Common"-deletion subject 4248.176