ProfileGDS1065 / 210966_x_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% 74% 79% 77% 77% 72% 70% 80% 80% 77% 74% 80% 80% 75% 75% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1139.675
GSM24653Normal subject 2119.574
GSM24654Normal subject 3211.879
GSM24655A3243G-MELAS subject 195.677
GSM24656A3243G-MELAS subject 2148.477
GSM24657A3243G-MELAS subject 3181.272
GSM24658A3243G-MELAS subject 497.170
GSM24659A3243G-PEO subject 1131.280
GSM24660A3243G-PEO subject 2159.280
GSM24661A3243G-PEO subject 3103.777
GSM24662A3243G-PEO subject 4102.974
GSM24663mtDNA "Common"-deletion subject 1188.180
GSM24664mtDNA "Common"-deletion subject 2312.880
GSM24665mtDNA "Common"-deletion subject 3209.975
GSM24666mtDNA "Common"-deletion subject 423075