ProfileGDS1065 / 222044_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 75% 70% 61% 68% 69% 75% 59% 75% 70% 77% 78% 74% 70% 71% 73% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 113775
GSM24653Normal subject 298.170
GSM24654Normal subject 386.361
GSM24655A3243G-MELAS subject 16468
GSM24656A3243G-MELAS subject 298.769
GSM24657A3243G-MELAS subject 3210.975
GSM24658A3243G-MELAS subject 456.659
GSM24659A3243G-PEO subject 1101.475
GSM24660A3243G-PEO subject 293.670
GSM24661A3243G-PEO subject 3101.577
GSM24662A3243G-PEO subject 4130.178
GSM24663mtDNA "Common"-deletion subject 1132.374
GSM24664mtDNA "Common"-deletion subject 218470
GSM24665mtDNA "Common"-deletion subject 3162.471
GSM24666mtDNA "Common"-deletion subject 4201.573