ProfileGDS1065 / 44654_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 89% 88% 84% 88% 86% 89% 88% 92% 91% 92% 92% 90% 85% 84% 81% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1405.389
GSM24653Normal subject 2304.688
GSM24654Normal subject 3300.784
GSM24655A3243G-MELAS subject 1203.588
GSM24656A3243G-MELAS subject 2279.586
GSM24657A3243G-MELAS subject 3591.589
GSM24658A3243G-MELAS subject 4311.388
GSM24659A3243G-PEO subject 1375.892
GSM24660A3243G-PEO subject 2394.791
GSM24661A3243G-PEO subject 3332.992
GSM24662A3243G-PEO subject 4417.392
GSM24663mtDNA "Common"-deletion subject 1455.790
GSM24664mtDNA "Common"-deletion subject 245085
GSM24665mtDNA "Common"-deletion subject 3383.384
GSM24666mtDNA "Common"-deletion subject 433981