ProfileGDS1065 / 215667_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 80% 77% 78% 76% 66% 75% 74% 75% 71% 73% 73% 80% 74% 70% 68% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1189.980
GSM24653Normal subject 2143.377
GSM24654Normal subject 3201.978
GSM24655A3243G-MELAS subject 190.776
GSM24656A3243G-MELAS subject 287.966
GSM24657A3243G-MELAS subject 3212.275
GSM24658A3243G-MELAS subject 4119.374
GSM24659A3243G-PEO subject 1102.375
GSM24660A3243G-PEO subject 295.671
GSM24661A3243G-PEO subject 382.373
GSM24662A3243G-PEO subject 498.273
GSM24663mtDNA "Common"-deletion subject 1194.380
GSM24664mtDNA "Common"-deletion subject 2224.374
GSM24665mtDNA "Common"-deletion subject 3159.970
GSM24666mtDNA "Common"-deletion subject 4156.868