ProfileGDS1065 / 208760_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% 83% 74% 77% 76% 82% 83% 76% 83% 83% 83% 74% 79% 82% 77% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1218.182
GSM24653Normal subject 2203.483
GSM24654Normal subject 3160.674
GSM24655A3243G-MELAS subject 198.577
GSM24656A3243G-MELAS subject 2142.676
GSM24657A3243G-MELAS subject 333582
GSM24658A3243G-MELAS subject 4204.483
GSM24659A3243G-PEO subject 1106.576
GSM24660A3243G-PEO subject 2195.783
GSM24661A3243G-PEO subject 3154.283
GSM24662A3243G-PEO subject 4185.783
GSM24663mtDNA "Common"-deletion subject 1128.674
GSM24664mtDNA "Common"-deletion subject 2299.979
GSM24665mtDNA "Common"-deletion subject 3334.282
GSM24666mtDNA "Common"-deletion subject 4252.477