ProfileGDS1065 / 202091_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 19% 52% 27% 39% 30% 20% 18% 24% 20% 12% 30% 30% 27% 36% 33% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 18.319
GSM24653Normal subject 245.952
GSM24654Normal subject 316.127
GSM24655A3243G-MELAS subject 120.639
GSM24656A3243G-MELAS subject 219.230
GSM24657A3243G-MELAS subject 311.920
GSM24658A3243G-MELAS subject 46.418
GSM24659A3243G-PEO subject 111.224
GSM24660A3243G-PEO subject 2920
GSM24661A3243G-PEO subject 33.812
GSM24662A3243G-PEO subject 415.230
GSM24663mtDNA "Common"-deletion subject 11730
GSM24664mtDNA "Common"-deletion subject 227.127
GSM24665mtDNA "Common"-deletion subject 335.436
GSM24666mtDNA "Common"-deletion subject 429.233