ProfileGDS1065 / 206699_x_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 8% 2% 9% 3% 27% 15% 7% 11% 3% 9% 3% 17% 15% 9% 13% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 13.68
GSM24653Normal subject 21.42
GSM24654Normal subject 34.29
GSM24655A3243G-MELAS subject 11.73
GSM24656A3243G-MELAS subject 216.327
GSM24657A3243G-MELAS subject 38.515
GSM24658A3243G-MELAS subject 42.57
GSM24659A3243G-PEO subject 14.811
GSM24660A3243G-PEO subject 21.83
GSM24661A3243G-PEO subject 339
GSM24662A3243G-PEO subject 41.73
GSM24663mtDNA "Common"-deletion subject 17.417
GSM24664mtDNA "Common"-deletion subject 211.215
GSM24665mtDNA "Common"-deletion subject 35.49
GSM24666mtDNA "Common"-deletion subject 4713