ProfileGDS1065 / 207639_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 30% 56% 62% 29% 51% 42% 29% 30% 40% 31% 52% 40% 20% 32% 28% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 117.830
GSM24653Normal subject 253.256
GSM24654Normal subject 387.862
GSM24655A3243G-MELAS subject 112.729
GSM24656A3243G-MELAS subject 249.851
GSM24657A3243G-MELAS subject 345.842
GSM24658A3243G-MELAS subject 413.929
GSM24659A3243G-PEO subject 116.230
GSM24660A3243G-PEO subject 227.640
GSM24661A3243G-PEO subject 312.931
GSM24662A3243G-PEO subject 440.752
GSM24663mtDNA "Common"-deletion subject 129.440
GSM24664mtDNA "Common"-deletion subject 216.420
GSM24665mtDNA "Common"-deletion subject 329.232
GSM24666mtDNA "Common"-deletion subject 421.628