ProfileGDS1065 / 209330_s_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 77% 76% 81% 83% 84% 83% 84% 75% 81% 79% 80% 79% 78% 85% 85% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1154.577
GSM24653Normal subject 2136.676
GSM24654Normal subject 3245.181
GSM24655A3243G-MELAS subject 1139.583
GSM24656A3243G-MELAS subject 2236.184
GSM24657A3243G-MELAS subject 3359.383
GSM24658A3243G-MELAS subject 4221.384
GSM24659A3243G-PEO subject 1100.575
GSM24660A3243G-PEO subject 2165.481
GSM24661A3243G-PEO subject 311579
GSM24662A3243G-PEO subject 4144.380
GSM24663mtDNA "Common"-deletion subject 1176.979
GSM24664mtDNA "Common"-deletion subject 2281.778
GSM24665mtDNA "Common"-deletion subject 3406.285
GSM24666mtDNA "Common"-deletion subject 4465.985