ProfileGDS1065 / 207205_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 52% 58% 60% 66% 49% 44% 51% 56% 57% 57% 57% 64% 54% 61% 65% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 148.252
GSM24653Normal subject 257.758
GSM24654Normal subject 380.860
GSM24655A3243G-MELAS subject 157.966
GSM24656A3243G-MELAS subject 24649
GSM24657A3243G-MELAS subject 350.244
GSM24658A3243G-MELAS subject 44151
GSM24659A3243G-PEO subject 146.456
GSM24660A3243G-PEO subject 254.657
GSM24661A3243G-PEO subject 341.657
GSM24662A3243G-PEO subject 449.457
GSM24663mtDNA "Common"-deletion subject 18264
GSM24664mtDNA "Common"-deletion subject 293.154
GSM24665mtDNA "Common"-deletion subject 3104.761
GSM24666mtDNA "Common"-deletion subject 4132.565