ProfileGDS1065 / 37278_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 79% 83% 72% 80% 77% 69% 76% 77% 69% 77% 78% 79% 73% 76% 79% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1171.679
GSM24653Normal subject 220383
GSM24654Normal subject 3145.472
GSM24655A3243G-MELAS subject 1110.780
GSM24656A3243G-MELAS subject 214677
GSM24657A3243G-MELAS subject 3152.969
GSM24658A3243G-MELAS subject 4130.976
GSM24659A3243G-PEO subject 1111.577
GSM24660A3243G-PEO subject 287.669
GSM24661A3243G-PEO subject 3105.977
GSM24662A3243G-PEO subject 4130.878
GSM24663mtDNA "Common"-deletion subject 1181.979
GSM24664mtDNA "Common"-deletion subject 2219.373
GSM24665mtDNA "Common"-deletion subject 3213.676
GSM24666mtDNA "Common"-deletion subject 4291.379