ProfileGDS1065 / 214805_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 43% 54% 58% 45% 54% 49% 55% 59% 39% 51% 57% 42% 50% 51% 62% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 133.343
GSM24653Normal subject 250.754
GSM24654Normal subject 375.658
GSM24655A3243G-MELAS subject 126.845
GSM24656A3243G-MELAS subject 25654
GSM24657A3243G-MELAS subject 360.249
GSM24658A3243G-MELAS subject 448.155
GSM24659A3243G-PEO subject 153.359
GSM24660A3243G-PEO subject 225.939
GSM24661A3243G-PEO subject 332.251
GSM24662A3243G-PEO subject 449.157
GSM24663mtDNA "Common"-deletion subject 132.142
GSM24664mtDNA "Common"-deletion subject 279.750
GSM24665mtDNA "Common"-deletion subject 367.451
GSM24666mtDNA "Common"-deletion subject 411262