ProfileGDS1065 / 216961_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 32% 39% 35% 46% 40% 59% 44% 43% 13% 51% 48% 53% 35% 34% 29% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 119.432
GSM24653Normal subject 227.339
GSM24654Normal subject 326.435
GSM24655A3243G-MELAS subject 127.546
GSM24656A3243G-MELAS subject 231.140
GSM24657A3243G-MELAS subject 395.659
GSM24658A3243G-MELAS subject 430.844
GSM24659A3243G-PEO subject 129.343
GSM24660A3243G-PEO subject 25.413
GSM24661A3243G-PEO subject 332.551
GSM24662A3243G-PEO subject 434.248
GSM24663mtDNA "Common"-deletion subject 152.153
GSM24664mtDNA "Common"-deletion subject 240.635
GSM24665mtDNA "Common"-deletion subject 331.934
GSM24666mtDNA "Common"-deletion subject 423.329