ProfileGDS1065 / 218591_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 34% 32% 33% 40% 36% 36% 29% 21% 31% 38% 43% 39% 26% 30% 32% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 122.134
GSM24653Normal subject 219.132
GSM24654Normal subject 323.433
GSM24655A3243G-MELAS subject 121.940
GSM24656A3243G-MELAS subject 226.736
GSM24657A3243G-MELAS subject 333.136
GSM24658A3243G-MELAS subject 414.129
GSM24659A3243G-PEO subject 19.121
GSM24660A3243G-PEO subject 217.631
GSM24661A3243G-PEO subject 318.738
GSM24662A3243G-PEO subject 42843
GSM24663mtDNA "Common"-deletion subject 127.439
GSM24664mtDNA "Common"-deletion subject 224.226
GSM24665mtDNA "Common"-deletion subject 326.230
GSM24666mtDNA "Common"-deletion subject 428.732