ProfileGDS1065 / 210017_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 44% 43% 32% 30% 42% 45% 49% 38% 35% 42% 30% 41% 52% 50% 57% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 135.244
GSM24653Normal subject 232.543
GSM24654Normal subject 322.932
GSM24655A3243G-MELAS subject 113.630
GSM24656A3243G-MELAS subject 234.742
GSM24657A3243G-MELAS subject 351.445
GSM24658A3243G-MELAS subject 437.749
GSM24659A3243G-PEO subject 123.738
GSM24660A3243G-PEO subject 221.635
GSM24661A3243G-PEO subject 322.542
GSM24662A3243G-PEO subject 415.230
GSM24663mtDNA "Common"-deletion subject 131.141
GSM24664mtDNA "Common"-deletion subject 284.452
GSM24665mtDNA "Common"-deletion subject 365.850
GSM24666mtDNA "Common"-deletion subject 490.357