ProfileGDS1065 / 214954_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 28% 18% 32% 26% 27% 27% 25% 25% 26% 34% 17% 34% 16% 19% 23% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 115.528
GSM24653Normal subject 27.718
GSM24654Normal subject 322.232
GSM24655A3243G-MELAS subject 110.526
GSM24656A3243G-MELAS subject 216.127
GSM24657A3243G-MELAS subject 32027
GSM24658A3243G-MELAS subject 410.425
GSM24659A3243G-PEO subject 111.725
GSM24660A3243G-PEO subject 21326
GSM24661A3243G-PEO subject 314.834
GSM24662A3243G-PEO subject 46.417
GSM24663mtDNA "Common"-deletion subject 121.534
GSM24664mtDNA "Common"-deletion subject 211.916
GSM24665mtDNA "Common"-deletion subject 311.919
GSM24666mtDNA "Common"-deletion subject 416.323