ProfileGDS1065 / 203956_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 83% 88% 81% 76% 89% 90% 86% 90% 88% 92% 92% 88% 86% 85% 90% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1226.883
GSM24653Normal subject 2313.888
GSM24654Normal subject 3246.381
GSM24655A3243G-MELAS subject 192.876
GSM24656A3243G-MELAS subject 2341.989
GSM24657A3243G-MELAS subject 3710.290
GSM24658A3243G-MELAS subject 4252.786
GSM24659A3243G-PEO subject 1268.390
GSM24660A3243G-PEO subject 2298.188
GSM24661A3243G-PEO subject 3337.992
GSM24662A3243G-PEO subject 4421.592
GSM24663mtDNA "Common"-deletion subject 1361.788
GSM24664mtDNA "Common"-deletion subject 2504.686
GSM24665mtDNA "Common"-deletion subject 3426.385
GSM24666mtDNA "Common"-deletion subject 4719.490