ProfileGDS1065 / 213853_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 79% 87% 85% 89% 89% 85% 85% 85% 88% 82% 80% 86% 89% 87% 86% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1176.379
GSM24653Normal subject 2274.787
GSM24654Normal subject 3339.485
GSM24655A3243G-MELAS subject 1212.889
GSM24656A3243G-MELAS subject 2349.989
GSM24657A3243G-MELAS subject 3432.785
GSM24658A3243G-MELAS subject 4241.185
GSM24659A3243G-PEO subject 1173.885
GSM24660A3243G-PEO subject 2281.888
GSM24661A3243G-PEO subject 3144.182
GSM24662A3243G-PEO subject 4143.280
GSM24663mtDNA "Common"-deletion subject 129486
GSM24664mtDNA "Common"-deletion subject 2652.289
GSM24665mtDNA "Common"-deletion subject 346887
GSM24666mtDNA "Common"-deletion subject 4488.186