ProfileGDS1065 / 214966_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 12% 11% 6% 4% 8% 4% 7% 6% 8% 6% 16% 7% 2% 4% 7% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 14.812
GSM24653Normal subject 24.711
GSM24654Normal subject 336
GSM24655A3243G-MELAS subject 11.84
GSM24656A3243G-MELAS subject 24.18
GSM24657A3243G-MELAS subject 32.64
GSM24658A3243G-MELAS subject 42.47
GSM24659A3243G-PEO subject 13.16
GSM24660A3243G-PEO subject 23.68
GSM24661A3243G-PEO subject 32.16
GSM24662A3243G-PEO subject 46.116
GSM24663mtDNA "Common"-deletion subject 13.37
GSM24664mtDNA "Common"-deletion subject 22.92
GSM24665mtDNA "Common"-deletion subject 334
GSM24666mtDNA "Common"-deletion subject 43.97