ProfileGDS1065 / 220099_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 82% 85% 87% 83% 87% 87% 86% 85% 84% 81% 82% 83% 86% 85% 88% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1210.982
GSM24653Normal subject 223685
GSM24654Normal subject 3410.187
GSM24655A3243G-MELAS subject 1138.783
GSM24656A3243G-MELAS subject 2290.287
GSM24657A3243G-MELAS subject 3488.987
GSM24658A3243G-MELAS subject 4266.486
GSM24659A3243G-PEO subject 1173.185
GSM24660A3243G-PEO subject 2210.884
GSM24661A3243G-PEO subject 3134.481
GSM24662A3243G-PEO subject 4168.382
GSM24663mtDNA "Common"-deletion subject 1225.783
GSM24664mtDNA "Common"-deletion subject 247286
GSM24665mtDNA "Common"-deletion subject 342185
GSM24666mtDNA "Common"-deletion subject 4624.888