ProfileGDS1065 / 219431_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 82% 80% 75% 78% 81% 84% 74% 83% 82% 81% 86% 82% 81% 79% 82% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1218.382
GSM24653Normal subject 2169.180
GSM24654Normal subject 3171.875
GSM24655A3243G-MELAS subject 1101.978
GSM24656A3243G-MELAS subject 2189.281
GSM24657A3243G-MELAS subject 3369.484
GSM24658A3243G-MELAS subject 4117.374
GSM24659A3243G-PEO subject 1154.683
GSM24660A3243G-PEO subject 2181.182
GSM24661A3243G-PEO subject 3130.381
GSM24662A3243G-PEO subject 4229.986
GSM24663mtDNA "Common"-deletion subject 1216.482
GSM24664mtDNA "Common"-deletion subject 233381
GSM24665mtDNA "Common"-deletion subject 3259.279
GSM24666mtDNA "Common"-deletion subject 4371.482