ProfileGDS1065 / 65133_i_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 33% 21% 32% 16% 31% 28% 35% 25% 31% 29% 32% 30% 20% 32% 20% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 120.733
GSM24653Normal subject 29.121
GSM24654Normal subject 322.832
GSM24655A3243G-MELAS subject 15.516
GSM24656A3243G-MELAS subject 22131
GSM24657A3243G-MELAS subject 321.828
GSM24658A3243G-MELAS subject 419.935
GSM24659A3243G-PEO subject 111.725
GSM24660A3243G-PEO subject 217.831
GSM24661A3243G-PEO subject 311.329
GSM24662A3243G-PEO subject 416.932
GSM24663mtDNA "Common"-deletion subject 116.730
GSM24664mtDNA "Common"-deletion subject 216.220
GSM24665mtDNA "Common"-deletion subject 328.432
GSM24666mtDNA "Common"-deletion subject 412.120