ProfileGDS1065 / 203050_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 74% 73% 73% 77% 66% 69% 65% 68% 64% 73% 69% 73% 72% 59% 60% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1131.174
GSM24653Normal subject 2111.973
GSM24654Normal subject 3152.773
GSM24655A3243G-MELAS subject 195.677
GSM24656A3243G-MELAS subject 288.266
GSM24657A3243G-MELAS subject 315869
GSM24658A3243G-MELAS subject 475.465
GSM24659A3243G-PEO subject 174.168
GSM24660A3243G-PEO subject 272.364
GSM24661A3243G-PEO subject 384.173
GSM24662A3243G-PEO subject 482.169
GSM24663mtDNA "Common"-deletion subject 1126.973
GSM24664mtDNA "Common"-deletion subject 2202.172
GSM24665mtDNA "Common"-deletion subject 393.259
GSM24666mtDNA "Common"-deletion subject 4104.260