ProfileGDS1065 / 202543_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 41% 49% 55% 50% 39% 49% 27% 32% 40% 50% 43% 45% 52% 56% 58% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 131.241
GSM24653Normal subject 241.649
GSM24654Normal subject 366.355
GSM24655A3243G-MELAS subject 132.150
GSM24656A3243G-MELAS subject 230.339
GSM24657A3243G-MELAS subject 362.149
GSM24658A3243G-MELAS subject 412.327
GSM24659A3243G-PEO subject 117.232
GSM24660A3243G-PEO subject 227.940
GSM24661A3243G-PEO subject 330.950
GSM24662A3243G-PEO subject 428.143
GSM24663mtDNA "Common"-deletion subject 13745
GSM24664mtDNA "Common"-deletion subject 283.852
GSM24665mtDNA "Common"-deletion subject 384.556
GSM24666mtDNA "Common"-deletion subject 496.158