ProfileGDS1065 / 205830_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 11% 29% 27% 36% 28% 42% 50% 46% 38% 35% 35% 68% 59% 25% 36% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 14.611
GSM24653Normal subject 216.529
GSM24654Normal subject 316.227
GSM24655A3243G-MELAS subject 118.136
GSM24656A3243G-MELAS subject 217.528
GSM24657A3243G-MELAS subject 345.842
GSM24658A3243G-MELAS subject 438.850
GSM24659A3243G-PEO subject 133.146
GSM24660A3243G-PEO subject 225.438
GSM24661A3243G-PEO subject 315.835
GSM24662A3243G-PEO subject 419.635
GSM24663mtDNA "Common"-deletion subject 197.868
GSM24664mtDNA "Common"-deletion subject 2112.959
GSM24665mtDNA "Common"-deletion subject 318.225
GSM24666mtDNA "Common"-deletion subject 43636