ProfileGDS1065 / 207016_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 84% 66% 75% 78% 66% 71% 70% 74% 79% 71% 75% 75% 82% 78% 75% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1240.384
GSM24653Normal subject 281.566
GSM24654Normal subject 3168.475
GSM24655A3243G-MELAS subject 1101.978
GSM24656A3243G-MELAS subject 28966
GSM24657A3243G-MELAS subject 3169.871
GSM24658A3243G-MELAS subject 498.170
GSM24659A3243G-PEO subject 194.274
GSM24660A3243G-PEO subject 2147.579
GSM24661A3243G-PEO subject 374.971
GSM24662A3243G-PEO subject 4108.175
GSM24663mtDNA "Common"-deletion subject 113975
GSM24664mtDNA "Common"-deletion subject 2355.482
GSM24665mtDNA "Common"-deletion subject 3240.178
GSM24666mtDNA "Common"-deletion subject 4227.175