ProfileGDS1065 / 220969_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 39% 40% 45% 32% 38% 36% 34% 31% 33% 37% 41% 36% 36% 36% 48% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 127.239
GSM24653Normal subject 228.340
GSM24654Normal subject 342.745
GSM24655A3243G-MELAS subject 115.232
GSM24656A3243G-MELAS subject 228.738
GSM24657A3243G-MELAS subject 334.436
GSM24658A3243G-MELAS subject 419.234
GSM24659A3243G-PEO subject 11731
GSM24660A3243G-PEO subject 219.433
GSM24661A3243G-PEO subject 317.237
GSM24662A3243G-PEO subject 425.641
GSM24663mtDNA "Common"-deletion subject 12436
GSM24664mtDNA "Common"-deletion subject 243.536
GSM24665mtDNA "Common"-deletion subject 334.936
GSM24666mtDNA "Common"-deletion subject 461.648