ProfileGDS1065 / 210443_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 70% 78% 63% 72% 73% 75% 74% 74% 80% 77% 76% 74% 76% 69% 65% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1103.870
GSM24653Normal subject 2148.378
GSM24654Normal subject 395.563
GSM24655A3243G-MELAS subject 177.372
GSM24656A3243G-MELAS subject 2119.973
GSM24657A3243G-MELAS subject 3207.275
GSM24658A3243G-MELAS subject 4119.174
GSM24659A3243G-PEO subject 196.274
GSM24660A3243G-PEO subject 2155.980
GSM24661A3243G-PEO subject 3105.277
GSM24662A3243G-PEO subject 4115.976
GSM24663mtDNA "Common"-deletion subject 1131.574
GSM24664mtDNA "Common"-deletion subject 2257.176
GSM24665mtDNA "Common"-deletion subject 3148.569
GSM24666mtDNA "Common"-deletion subject 4130.965