ProfileGDS1065 / 206614_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 49% 37% 27% 28% 46% 37% 31% 30% 48% 53% 48% 43% 22% 30% 39% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 142.449
GSM24653Normal subject 22437
GSM24654Normal subject 316.127
GSM24655A3243G-MELAS subject 111.928
GSM24656A3243G-MELAS subject 240.546
GSM24657A3243G-MELAS subject 33537
GSM24658A3243G-MELAS subject 415.731
GSM24659A3243G-PEO subject 115.630
GSM24660A3243G-PEO subject 238.148
GSM24661A3243G-PEO subject 336.253
GSM24662A3243G-PEO subject 434.448
GSM24663mtDNA "Common"-deletion subject 133.743
GSM24664mtDNA "Common"-deletion subject 219.122
GSM24665mtDNA "Common"-deletion subject 324.930
GSM24666mtDNA "Common"-deletion subject 441.139