ProfileGDS1065 / 209445_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 87% 89% 87% 86% 85% 80% 81% 74% 80% 82% 77% 81% 84% 89% 85% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1316.287
GSM24653Normal subject 2337.789
GSM24654Normal subject 3401.687
GSM24655A3243G-MELAS subject 117486
GSM24656A3243G-MELAS subject 225285
GSM24657A3243G-MELAS subject 3288.780
GSM24658A3243G-MELAS subject 4185.981
GSM24659A3243G-PEO subject 197.274
GSM24660A3243G-PEO subject 2157.280
GSM24661A3243G-PEO subject 3140.282
GSM24662A3243G-PEO subject 4122.377
GSM24663mtDNA "Common"-deletion subject 1204.981
GSM24664mtDNA "Common"-deletion subject 2418.284
GSM24665mtDNA "Common"-deletion subject 3625.889
GSM24666mtDNA "Common"-deletion subject 4450.785