ProfileGDS1065 / 217235_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 68% 67% 68% 67% 65% 34% 49% 69% 53% 75% 32% 56% 64% 52% 62% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 197.968
GSM24653Normal subject 286.767
GSM24654Normal subject 3117.268
GSM24655A3243G-MELAS subject 160.467
GSM24656A3243G-MELAS subject 28565
GSM24657A3243G-MELAS subject 330.934
GSM24658A3243G-MELAS subject 438.649
GSM24659A3243G-PEO subject 177.269
GSM24660A3243G-PEO subject 245.753
GSM24661A3243G-PEO subject 391.175
GSM24662A3243G-PEO subject 416.832
GSM24663mtDNA "Common"-deletion subject 15956
GSM24664mtDNA "Common"-deletion subject 2138.864
GSM24665mtDNA "Common"-deletion subject 370.652
GSM24666mtDNA "Common"-deletion subject 4114.962