ProfileGDS1065 / 211079_s_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 29% 44% 41% 21% 14% 25% 30% 38% 36% 16% 16% 9% 15% 37% 21% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 115.829
GSM24653Normal subject 233.444
GSM24654Normal subject 334.841
GSM24655A3243G-MELAS subject 17.521
GSM24656A3243G-MELAS subject 26.514
GSM24657A3243G-MELAS subject 316.825
GSM24658A3243G-MELAS subject 414.930
GSM24659A3243G-PEO subject 123.638
GSM24660A3243G-PEO subject 223.336
GSM24661A3243G-PEO subject 3516
GSM24662A3243G-PEO subject 45.916
GSM24663mtDNA "Common"-deletion subject 13.99
GSM24664mtDNA "Common"-deletion subject 210.815
GSM24665mtDNA "Common"-deletion subject 335.937
GSM24666mtDNA "Common"-deletion subject 413.721