ProfileGDS1065 / 207028_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% 19% 14% 13% 12% 8% 10% 19% 17% 20% 14% 20% 34% 17% 32% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 18.319
GSM24653Normal subject 28.219
GSM24654Normal subject 36.614
GSM24655A3243G-MELAS subject 14.513
GSM24656A3243G-MELAS subject 25.912
GSM24657A3243G-MELAS subject 34.58
GSM24658A3243G-MELAS subject 43.310
GSM24659A3243G-PEO subject 17.919
GSM24660A3243G-PEO subject 27.217
GSM24661A3243G-PEO subject 36.520
GSM24662A3243G-PEO subject 4514
GSM24663mtDNA "Common"-deletion subject 18.720
GSM24664mtDNA "Common"-deletion subject 238.734
GSM24665mtDNA "Common"-deletion subject 310.517
GSM24666mtDNA "Common"-deletion subject 42832