ProfileGDS1065 / 217774_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 95% 95% 93% 91% 94% 96% 95% 94% 95% 93% 94% 95% 95% 94% 95% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1865.195
GSM24653Normal subject 2785.695
GSM24654Normal subject 3825.193
GSM24655A3243G-MELAS subject 1265.191
GSM24656A3243G-MELAS subject 2678.194
GSM24657A3243G-MELAS subject 31708.196
GSM24658A3243G-MELAS subject 4799.995
GSM24659A3243G-PEO subject 1471.494
GSM24660A3243G-PEO subject 2766.595
GSM24661A3243G-PEO subject 3415.293
GSM24662A3243G-PEO subject 4628.794
GSM24663mtDNA "Common"-deletion subject 1903.295
GSM24664mtDNA "Common"-deletion subject 21512.495
GSM24665mtDNA "Common"-deletion subject 31236.694
GSM24666mtDNA "Common"-deletion subject 41687.995