ProfileGDS1065 / 203223_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 38% 38% 55% 32% 40% 32% 45% 38% 28% 51% 26% 40% 41% 36% 51% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 126.938
GSM24653Normal subject 226.238
GSM24654Normal subject 367.155
GSM24655A3243G-MELAS subject 114.632
GSM24656A3243G-MELAS subject 230.940
GSM24657A3243G-MELAS subject 32732
GSM24658A3243G-MELAS subject 432.145
GSM24659A3243G-PEO subject 123.138
GSM24660A3243G-PEO subject 214.928
GSM24661A3243G-PEO subject 333.251
GSM24662A3243G-PEO subject 411.926
GSM24663mtDNA "Common"-deletion subject 128.840
GSM24664mtDNA "Common"-deletion subject 253.941
GSM24665mtDNA "Common"-deletion subject 335.636
GSM24666mtDNA "Common"-deletion subject 468.751