ProfileGDS1065 / 210896_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 24% 48% 67% 50% 52% 11% 34% 23% 49% 49% 44% 30% 59% 52% 54% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 111.724
GSM24653Normal subject 239.648
GSM24654Normal subject 311067
GSM24655A3243G-MELAS subject 132.550
GSM24656A3243G-MELAS subject 250.952
GSM24657A3243G-MELAS subject 36.111
GSM24658A3243G-MELAS subject 419.234
GSM24659A3243G-PEO subject 110.823
GSM24660A3243G-PEO subject 240.449
GSM24661A3243G-PEO subject 33049
GSM24662A3243G-PEO subject 429.344
GSM24663mtDNA "Common"-deletion subject 116.730
GSM24664mtDNA "Common"-deletion subject 2114.859
GSM24665mtDNA "Common"-deletion subject 371.352
GSM24666mtDNA "Common"-deletion subject 477.154