ProfileGDS1065 / 214469_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 3% 4% 9% 8% 22% 2% 2% 2% 7% 6% 24% 4% 9% 8% 21% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 12.13
GSM24653Normal subject 22.34
GSM24654Normal subject 34.29
GSM24655A3243G-MELAS subject 13.18
GSM24656A3243G-MELAS subject 211.422
GSM24657A3243G-MELAS subject 32.12
GSM24658A3243G-MELAS subject 41.32
GSM24659A3243G-PEO subject 11.82
GSM24660A3243G-PEO subject 23.27
GSM24661A3243G-PEO subject 32.16
GSM24662A3243G-PEO subject 49.824
GSM24663mtDNA "Common"-deletion subject 12.44
GSM24664mtDNA "Common"-deletion subject 27.29
GSM24665mtDNA "Common"-deletion subject 35.18
GSM24666mtDNA "Common"-deletion subject 41321