ProfileGDS1065 / 208737_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 85% 85% 94% 87% 86% 81% 90% 84% 87% 65% 77% 82% 89% 89% 89% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1259.185
GSM24653Normal subject 2233.885
GSM24654Normal subject 3997.194
GSM24655A3243G-MELAS subject 117887
GSM24656A3243G-MELAS subject 2272.286
GSM24657A3243G-MELAS subject 3300.481
GSM24658A3243G-MELAS subject 4364.290
GSM24659A3243G-PEO subject 1169.684
GSM24660A3243G-PEO subject 225587
GSM24661A3243G-PEO subject 356.565
GSM24662A3243G-PEO subject 4122.877
GSM24663mtDNA "Common"-deletion subject 1221.582
GSM24664mtDNA "Common"-deletion subject 2668.589
GSM24665mtDNA "Common"-deletion subject 3600.389
GSM24666mtDNA "Common"-deletion subject 4646.589