ProfileGDS1065 / 205251_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 92% 70% 85% 83% 86% 91% 85% 86% 89% 86% 90% 87% 86% 91% 90% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1522.492
GSM24653Normal subject 297.170
GSM24654Normal subject 3329.985
GSM24655A3243G-MELAS subject 1132.383
GSM24656A3243G-MELAS subject 2266.886
GSM24657A3243G-MELAS subject 3751.891
GSM24658A3243G-MELAS subject 4244.685
GSM24659A3243G-PEO subject 1193.786
GSM24660A3243G-PEO subject 2326.889
GSM24661A3243G-PEO subject 3189.386
GSM24662A3243G-PEO subject 4341.990
GSM24663mtDNA "Common"-deletion subject 1325.787
GSM24664mtDNA "Common"-deletion subject 2481.386
GSM24665mtDNA "Common"-deletion subject 3727.591
GSM24666mtDNA "Common"-deletion subject 4777.490