ProfileGDS1065 / 206749_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 23% 47% 23% 34% 29% 27% 21% 14% 47% 17% 20% 21% 17% 42% 43% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 110.723
GSM24653Normal subject 238.447
GSM24654Normal subject 312.223
GSM24655A3243G-MELAS subject 116.934
GSM24656A3243G-MELAS subject 218.929
GSM24657A3243G-MELAS subject 319.327
GSM24658A3243G-MELAS subject 48.421
GSM24659A3243G-PEO subject 1614
GSM24660A3243G-PEO subject 236.247
GSM24661A3243G-PEO subject 35.317
GSM24662A3243G-PEO subject 47.520
GSM24663mtDNA "Common"-deletion subject 19.221
GSM24664mtDNA "Common"-deletion subject 213.517
GSM24665mtDNA "Common"-deletion subject 34642
GSM24666mtDNA "Common"-deletion subject 448.343