ProfileGDS1065 / 214766_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 47% 32% 51% 39% 46% 50% 49% 43% 45% 37% 45% 52% 46% 41% 48% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 139.247
GSM24653Normal subject 219.732
GSM24654Normal subject 355.551
GSM24655A3243G-MELAS subject 121.339
GSM24656A3243G-MELAS subject 24146
GSM24657A3243G-MELAS subject 36550
GSM24658A3243G-MELAS subject 438.649
GSM24659A3243G-PEO subject 128.943
GSM24660A3243G-PEO subject 234.545
GSM24661A3243G-PEO subject 317.237
GSM24662A3243G-PEO subject 431.445
GSM24663mtDNA "Common"-deletion subject 148.652
GSM24664mtDNA "Common"-deletion subject 266.346
GSM24665mtDNA "Common"-deletion subject 344.541
GSM24666mtDNA "Common"-deletion subject 459.948