ProfileGDS1065 / 221231_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 4% 6% 27% 4% 8% 6% 5% 15% 6% 13% 5% 6% 6% 3% 5% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 12.34
GSM24653Normal subject 236
GSM24654Normal subject 316.227
GSM24655A3243G-MELAS subject 12.14
GSM24656A3243G-MELAS subject 24.38
GSM24657A3243G-MELAS subject 33.76
GSM24658A3243G-MELAS subject 42.15
GSM24659A3243G-PEO subject 16.515
GSM24660A3243G-PEO subject 236
GSM24661A3243G-PEO subject 3413
GSM24662A3243G-PEO subject 42.15
GSM24663mtDNA "Common"-deletion subject 13.16
GSM24664mtDNA "Common"-deletion subject 24.96
GSM24665mtDNA "Common"-deletion subject 32.83
GSM24666mtDNA "Common"-deletion subject 43.45