ProfileGDS1065 / 206970_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 19% 15% 20% 18% 19% 13% 16% 14% 34% 14% 8% 23% 10% 25% 11% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 18.619
GSM24653Normal subject 26.215
GSM24654Normal subject 39.920
GSM24655A3243G-MELAS subject 16.218
GSM24656A3243G-MELAS subject 29.719
GSM24657A3243G-MELAS subject 3713
GSM24658A3243G-MELAS subject 45.516
GSM24659A3243G-PEO subject 15.814
GSM24660A3243G-PEO subject 220.334
GSM24661A3243G-PEO subject 34.514
GSM24662A3243G-PEO subject 438
GSM24663mtDNA "Common"-deletion subject 110.523
GSM24664mtDNA "Common"-deletion subject 27.510
GSM24665mtDNA "Common"-deletion subject 318.225
GSM24666mtDNA "Common"-deletion subject 46.211