ProfileGDS1065 / 218840_s_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 17% 13% 6% 15% 11% 8% 15% 18% 20% 9% 25% 23% 29% 19% 13% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 17.317
GSM24653Normal subject 25.413
GSM24654Normal subject 33.36
GSM24655A3243G-MELAS subject 15.115
GSM24656A3243G-MELAS subject 25.311
GSM24657A3243G-MELAS subject 34.38
GSM24658A3243G-MELAS subject 45.215
GSM24659A3243G-PEO subject 17.518
GSM24660A3243G-PEO subject 28.820
GSM24661A3243G-PEO subject 32.89
GSM24662A3243G-PEO subject 410.725
GSM24663mtDNA "Common"-deletion subject 110.423
GSM24664mtDNA "Common"-deletion subject 229.229
GSM24665mtDNA "Common"-deletion subject 31219
GSM24666mtDNA "Common"-deletion subject 46.813