ProfileGDS1065 / 206423_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 15% 63% 57% 39% 30% 30% 20% 51% 23% 36% 34% 15% 9% 19% 4% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 16.115
GSM24653Normal subject 273.163
GSM24654Normal subject 371.657
GSM24655A3243G-MELAS subject 120.939
GSM24656A3243G-MELAS subject 219.130
GSM24657A3243G-MELAS subject 324.230
GSM24658A3243G-MELAS subject 47.720
GSM24659A3243G-PEO subject 139.151
GSM24660A3243G-PEO subject 210.823
GSM24661A3243G-PEO subject 316.736
GSM24662A3243G-PEO subject 418.834
GSM24663mtDNA "Common"-deletion subject 16.315
GSM24664mtDNA "Common"-deletion subject 26.99
GSM24665mtDNA "Common"-deletion subject 311.719
GSM24666mtDNA "Common"-deletion subject 42.84