ProfileGDS1065 / 220717_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 20% 30% 1% 23% 20% 0% 15% 28% 26% 20% 23% 34% 15% 11% 20% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 19.120
GSM24653Normal subject 217.330
GSM24654Normal subject 30.71
GSM24655A3243G-MELAS subject 18.623
GSM24656A3243G-MELAS subject 210.320
GSM24657A3243G-MELAS subject 30.50
GSM24658A3243G-MELAS subject 45.215
GSM24659A3243G-PEO subject 114.528
GSM24660A3243G-PEO subject 213.326
GSM24661A3243G-PEO subject 36.520
GSM24662A3243G-PEO subject 49.423
GSM24663mtDNA "Common"-deletion subject 120.734
GSM24664mtDNA "Common"-deletion subject 211.315
GSM24665mtDNA "Common"-deletion subject 36.211
GSM24666mtDNA "Common"-deletion subject 412.520