ProfileGDS1065 / 214773_x_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 63% 66% 73% 71% 73% 72% 72% 67% 50% 55% 54% 72% 64% 61% 68% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 178.263
GSM24653Normal subject 28366
GSM24654Normal subject 3150.273
GSM24655A3243G-MELAS subject 172.371
GSM24656A3243G-MELAS subject 2118.673
GSM24657A3243G-MELAS subject 3182.972
GSM24658A3243G-MELAS subject 4110.472
GSM24659A3243G-PEO subject 169.567
GSM24660A3243G-PEO subject 241.750
GSM24661A3243G-PEO subject 33955
GSM24662A3243G-PEO subject 444.954
GSM24663mtDNA "Common"-deletion subject 1118.972
GSM24664mtDNA "Common"-deletion subject 2141.764
GSM24665mtDNA "Common"-deletion subject 3102.261
GSM24666mtDNA "Common"-deletion subject 4159.268