ProfileGDS1065 / 204507_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 15% 5% 29% 26% 20% 32% 37% 30% 29% 32% 27% 31% 24% 20% 30% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 16.115
GSM24653Normal subject 22.75
GSM24654Normal subject 318.429
GSM24655A3243G-MELAS subject 110.826
GSM24656A3243G-MELAS subject 210.120
GSM24657A3243G-MELAS subject 326.732
GSM24658A3243G-MELAS subject 422.637
GSM24659A3243G-PEO subject 116.130
GSM24660A3243G-PEO subject 215.229
GSM24661A3243G-PEO subject 313.532
GSM24662A3243G-PEO subject 412.527
GSM24663mtDNA "Common"-deletion subject 117.931
GSM24664mtDNA "Common"-deletion subject 22224
GSM24665mtDNA "Common"-deletion subject 312.620
GSM24666mtDNA "Common"-deletion subject 425.430