ProfileGDS1065 / 221878_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 59% 66% 62% 57% 60% 65% 59% 46% 49% 63% 30% 66% 61% 69% 65% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 163.859
GSM24653Normal subject 283.666
GSM24654Normal subject 388.562
GSM24655A3243G-MELAS subject 141.257
GSM24656A3243G-MELAS subject 270.660
GSM24657A3243G-MELAS subject 312565
GSM24658A3243G-MELAS subject 456.859
GSM24659A3243G-PEO subject 132.346
GSM24660A3243G-PEO subject 239.249
GSM24661A3243G-PEO subject 353.463
GSM24662A3243G-PEO subject 414.630
GSM24663mtDNA "Common"-deletion subject 188.666
GSM24664mtDNA "Common"-deletion subject 2123.961
GSM24665mtDNA "Common"-deletion subject 3148.169
GSM24666mtDNA "Common"-deletion subject 4131.465