ProfileGDS1065 / 202668_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 80% 81% 82% 79% 80% 79% 80% 83% 72% 78% 76% 77% 82% 80% 84% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1179.380
GSM24653Normal subject 2186.181
GSM24654Normal subject 3257.182
GSM24655A3243G-MELAS subject 1106.779
GSM24656A3243G-MELAS subject 2183.280
GSM24657A3243G-MELAS subject 3265.479
GSM24658A3243G-MELAS subject 4172.780
GSM24659A3243G-PEO subject 1152.683
GSM24660A3243G-PEO subject 2102.872
GSM24661A3243G-PEO subject 3109.178
GSM24662A3243G-PEO subject 4118.276
GSM24663mtDNA "Common"-deletion subject 1159.977
GSM24664mtDNA "Common"-deletion subject 2357.582
GSM24665mtDNA "Common"-deletion subject 3278.380
GSM24666mtDNA "Common"-deletion subject 4406.284