ProfileGDS1065 / 213680_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 59% 58% 54% 50% 59% 49% 57% 58% 62% 60% 61% 56% 60% 58% 53% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 165.459
GSM24653Normal subject 258.158
GSM24654Normal subject 364.154
GSM24655A3243G-MELAS subject 132.350
GSM24656A3243G-MELAS subject 266.959
GSM24657A3243G-MELAS subject 361.649
GSM24658A3243G-MELAS subject 452.557
GSM24659A3243G-PEO subject 149.758
GSM24660A3243G-PEO subject 264.762
GSM24661A3243G-PEO subject 346.860
GSM24662A3243G-PEO subject 458.561
GSM24663mtDNA "Common"-deletion subject 157.456
GSM24664mtDNA "Common"-deletion subject 2119.760
GSM24665mtDNA "Common"-deletion subject 390.958
GSM24666mtDNA "Common"-deletion subject 476.553