ProfileGDS1065 / 218351_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% 66% 87% 81% 83% 76% 79% 77% 81% 69% 67% 84% 86% 87% 83% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1205.182
GSM24653Normal subject 282.966
GSM24654Normal subject 3406.987
GSM24655A3243G-MELAS subject 1121.781
GSM24656A3243G-MELAS subject 2210.783
GSM24657A3243G-MELAS subject 3229.676
GSM24658A3243G-MELAS subject 4159.979
GSM24659A3243G-PEO subject 1111.277
GSM24660A3243G-PEO subject 2166.981
GSM24661A3243G-PEO subject 368.669
GSM24662A3243G-PEO subject 474.467
GSM24663mtDNA "Common"-deletion subject 1249.884
GSM24664mtDNA "Common"-deletion subject 2501.686
GSM24665mtDNA "Common"-deletion subject 3503.487
GSM24666mtDNA "Common"-deletion subject 4385.283