ProfileGDS1065 / 215535_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 90% 86% 91% 90% 88% 87% 87% 90% 88% 87% 89% 87% 85% 89% 84% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1440.490
GSM24653Normal subject 2261.486
GSM24654Normal subject 3591.191
GSM24655A3243G-MELAS subject 1236.990
GSM24656A3243G-MELAS subject 2322.988
GSM24657A3243G-MELAS subject 349487
GSM24658A3243G-MELAS subject 4286.987
GSM24659A3243G-PEO subject 1265.690
GSM24660A3243G-PEO subject 2292.288
GSM24661A3243G-PEO subject 3192.787
GSM24662A3243G-PEO subject 4297.689
GSM24663mtDNA "Common"-deletion subject 1327.687
GSM24664mtDNA "Common"-deletion subject 2447.485
GSM24665mtDNA "Common"-deletion subject 3631.189
GSM24666mtDNA "Common"-deletion subject 4433.484