ProfileGDS1065 / 221313_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 11% 12% 18% 9% 11% 10% 18% 18% 18% 16% 19% 18% 15% 20% 18% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 14.611
GSM24653Normal subject 25.112
GSM24654Normal subject 38.618
GSM24655A3243G-MELAS subject 13.39
GSM24656A3243G-MELAS subject 25.511
GSM24657A3243G-MELAS subject 35.510
GSM24658A3243G-MELAS subject 46.618
GSM24659A3243G-PEO subject 17.818
GSM24660A3243G-PEO subject 27.618
GSM24661A3243G-PEO subject 35.116
GSM24662A3243G-PEO subject 4719
GSM24663mtDNA "Common"-deletion subject 17.818
GSM24664mtDNA "Common"-deletion subject 210.915
GSM24665mtDNA "Common"-deletion subject 312.620
GSM24666mtDNA "Common"-deletion subject 410.318