ProfileGDS1065 / 209813_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 9% 3% 10% 8% 11% 11% 10% 4% 8% 7% 12% 5% 9% 7% 9% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 149
GSM24653Normal subject 223
GSM24654Normal subject 34.610
GSM24655A3243G-MELAS subject 138
GSM24656A3243G-MELAS subject 25.411
GSM24657A3243G-MELAS subject 35.911
GSM24658A3243G-MELAS subject 43.310
GSM24659A3243G-PEO subject 12.34
GSM24660A3243G-PEO subject 23.68
GSM24661A3243G-PEO subject 32.57
GSM24662A3243G-PEO subject 44.412
GSM24663mtDNA "Common"-deletion subject 12.65
GSM24664mtDNA "Common"-deletion subject 27.29
GSM24665mtDNA "Common"-deletion subject 34.37
GSM24666mtDNA "Common"-deletion subject 459