ProfileGDS1065 / 218488_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 94% 93% 93% 94% 93% 92% 93% 93% 93% 93% 93% 93% 93% 93% 92% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1755.294
GSM24653Normal subject 2604.293
GSM24654Normal subject 3753.993
GSM24655A3243G-MELAS subject 139894
GSM24656A3243G-MELAS subject 2587.793
GSM24657A3243G-MELAS subject 3917.592
GSM24658A3243G-MELAS subject 4552.593
GSM24659A3243G-PEO subject 1391.793
GSM24660A3243G-PEO subject 2526.193
GSM24661A3243G-PEO subject 3392.693
GSM24662A3243G-PEO subject 4497.293
GSM24663mtDNA "Common"-deletion subject 1669.493
GSM24664mtDNA "Common"-deletion subject 21112.293
GSM24665mtDNA "Common"-deletion subject 31046.993
GSM24666mtDNA "Common"-deletion subject 4937.492