ProfileGDS1065 / 205969_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 11% 12% 13% 19% 13% 17% 1% 15% 12% 33% 19% 19% 13% 12% 3% sort by genotype/variation sort by disease state Gene Expression Profile
Graph caption help
SampleTitleValueRank
GSM24652Normal subject 14.611
GSM24653Normal subject 24.912
GSM24654Normal subject 35.813
GSM24655A3243G-MELAS subject 16.619
GSM24656A3243G-MELAS subject 26.213
GSM24657A3243G-MELAS subject 39.717
GSM24658A3243G-MELAS subject 411
GSM24659A3243G-PEO subject 16.315
GSM24660A3243G-PEO subject 2512
GSM24661A3243G-PEO subject 313.833
GSM24662A3243G-PEO subject 47.319
GSM24663mtDNA "Common"-deletion subject 18.219
GSM24664mtDNA "Common"-deletion subject 29.313
GSM24665mtDNA "Common"-deletion subject 37.112
GSM24666mtDNA "Common"-deletion subject 42.33