ProfileGDS1065 / 201152_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 93% 88% 97% 86% 96% 94% 96% 84% 93% 86% 85% 90% 96% 95% 96% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1684.393
GSM24653Normal subject 2298.188
GSM24654Normal subject 32259.997
GSM24655A3243G-MELAS subject 1173.186
GSM24656A3243G-MELAS subject 21044.996
GSM24657A3243G-MELAS subject 31106.194
GSM24658A3243G-MELAS subject 41028.696
GSM24659A3243G-PEO subject 1172.284
GSM24660A3243G-PEO subject 2531.493
GSM24661A3243G-PEO subject 3187.386
GSM24662A3243G-PEO subject 4206.985
GSM24663mtDNA "Common"-deletion subject 1436.690
GSM24664mtDNA "Common"-deletion subject 21960.396
GSM24665mtDNA "Common"-deletion subject 31517.795
GSM24666mtDNA "Common"-deletion subject 42240.196