ProfileGDS1065 / 212237_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 80% 79% 78% 80% 80% 74% 77% 79% 77% 68% 76% 79% 77% 73% 75% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1189.180
GSM24653Normal subject 2155.879
GSM24654Normal subject 3202.178
GSM24655A3243G-MELAS subject 1110.780
GSM24656A3243G-MELAS subject 218180
GSM24657A3243G-MELAS subject 3201.974
GSM24658A3243G-MELAS subject 4143.877
GSM24659A3243G-PEO subject 1125.479
GSM24660A3243G-PEO subject 2130.977
GSM24661A3243G-PEO subject 366.168
GSM24662A3243G-PEO subject 4115.276
GSM24663mtDNA "Common"-deletion subject 117779
GSM24664mtDNA "Common"-deletion subject 2261.977
GSM24665mtDNA "Common"-deletion subject 3178.973
GSM24666mtDNA "Common"-deletion subject 422675