ProfileGDS1065 / 203727_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 81% 82% 70% 73% 77% 83% 83% 84% 81% 84% 82% 81% 81% 69% 76% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1203.681
GSM24653Normal subject 2192.782
GSM24654Normal subject 313170
GSM24655A3243G-MELAS subject 18073
GSM24656A3243G-MELAS subject 215277
GSM24657A3243G-MELAS subject 3360.683
GSM24658A3243G-MELAS subject 4209.283
GSM24659A3243G-PEO subject 1164.984
GSM24660A3243G-PEO subject 2164.981
GSM24661A3243G-PEO subject 3157.584
GSM24662A3243G-PEO subject 4171.282
GSM24663mtDNA "Common"-deletion subject 1199.481
GSM24664mtDNA "Common"-deletion subject 2332.881
GSM24665mtDNA "Common"-deletion subject 3152.469
GSM24666mtDNA "Common"-deletion subject 424676