ProfileGDS1065 / 210679_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 84% 82% 68% 79% 85% 80% 74% 87% 82% 90% 90% 78% 77% 77% 82% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1236.984
GSM24653Normal subject 2194.682
GSM24654Normal subject 311768
GSM24655A3243G-MELAS subject 1105.979
GSM24656A3243G-MELAS subject 2241.885
GSM24657A3243G-MELAS subject 3290.780
GSM24658A3243G-MELAS subject 412174
GSM24659A3243G-PEO subject 1200.987
GSM24660A3243G-PEO subject 2180.882
GSM24661A3243G-PEO subject 3271.890
GSM24662A3243G-PEO subject 431590
GSM24663mtDNA "Common"-deletion subject 1171.178
GSM24664mtDNA "Common"-deletion subject 2264.377
GSM24665mtDNA "Common"-deletion subject 3229.477
GSM24666mtDNA "Common"-deletion subject 4356.882