ProfileGDS1065 / 219771_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% 28% 13% 36% 34% 26% 4% 40% 7% 21% 38% 38% 27% 15% 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 317.328
GSM24655A3243G-MELAS subject 14.713
GSM24656A3243G-MELAS subject 22636
GSM24657A3243G-MELAS subject 33034
GSM24658A3243G-MELAS subject 411.226
GSM24659A3243G-PEO subject 12.24
GSM24660A3243G-PEO subject 227.140
GSM24661A3243G-PEO subject 32.47
GSM24662A3243G-PEO subject 48.221
GSM24663mtDNA "Common"-deletion subject 127.138
GSM24664mtDNA "Common"-deletion subject 248.838
GSM24665mtDNA "Common"-deletion subject 321.527
GSM24666mtDNA "Common"-deletion subject 48.515