ProfileGDS1065 / 205229_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 35% 51% 40% 52% 40% 60% 35% 47% 37% 44% 53% 41% 46% 35% 45% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 123.435
GSM24653Normal subject 244.951
GSM24654Normal subject 333.140
GSM24655A3243G-MELAS subject 134.352
GSM24656A3243G-MELAS subject 23240
GSM24657A3243G-MELAS subject 398.760
GSM24658A3243G-MELAS subject 420.435
GSM24659A3243G-PEO subject 133.747
GSM24660A3243G-PEO subject 224.437
GSM24661A3243G-PEO subject 324.144
GSM24662A3243G-PEO subject 443.153
GSM24663mtDNA "Common"-deletion subject 130.941
GSM24664mtDNA "Common"-deletion subject 268.446
GSM24665mtDNA "Common"-deletion subject 333.635
GSM24666mtDNA "Common"-deletion subject 452.845