ProfileGDS1065 / 203922_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 44% 48% 45% 49% 47% 41% 52% 47% 55% 29% 37% 45% 41% 46% 35% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 134.744
GSM24653Normal subject 239.248
GSM24654Normal subject 342.245
GSM24655A3243G-MELAS subject 131.349
GSM24656A3243G-MELAS subject 242.447
GSM24657A3243G-MELAS subject 342.941
GSM24658A3243G-MELAS subject 443.352
GSM24659A3243G-PEO subject 133.847
GSM24660A3243G-PEO subject 250.455
GSM24661A3243G-PEO subject 311.329
GSM24662A3243G-PEO subject 422.137
GSM24663mtDNA "Common"-deletion subject 136.845
GSM24664mtDNA "Common"-deletion subject 253.841
GSM24665mtDNA "Common"-deletion subject 355.346
GSM24666mtDNA "Common"-deletion subject 433.835