ProfileGDS1065 / 202024_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 74% 65% 78% 78% 77% 78% 77% 82% 80% 75% 76% 73% 77% 73% 72% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 112974
GSM24653Normal subject 280.165
GSM24654Normal subject 3208.778
GSM24655A3243G-MELAS subject 1103.178
GSM24656A3243G-MELAS subject 2153.477
GSM24657A3243G-MELAS subject 325778
GSM24658A3243G-MELAS subject 4143.677
GSM24659A3243G-PEO subject 114682
GSM24660A3243G-PEO subject 2152.780
GSM24661A3243G-PEO subject 393.475
GSM24662A3243G-PEO subject 4119.976
GSM24663mtDNA "Common"-deletion subject 1122.473
GSM24664mtDNA "Common"-deletion subject 2270.477
GSM24665mtDNA "Common"-deletion subject 3182.173
GSM24666mtDNA "Common"-deletion subject 419272