ProfileGDS1065 / 207232_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 15% 19% 56% 7% 17% 12% 14% 19% 19% 12% 8% 23% 18% 28% 11% sort by genotype/variation sort by disease state Gene Expression Profile
Graph caption help
SampleTitleValueRank
GSM24652Normal subject 16.215
GSM24653Normal subject 2819
GSM24654Normal subject 369.856
GSM24655A3243G-MELAS subject 12.97
GSM24656A3243G-MELAS subject 28.217
GSM24657A3243G-MELAS subject 36.212
GSM24658A3243G-MELAS subject 44.714
GSM24659A3243G-PEO subject 18.119
GSM24660A3243G-PEO subject 28.519
GSM24661A3243G-PEO subject 33.712
GSM24662A3243G-PEO subject 43.18
GSM24663mtDNA "Common"-deletion subject 110.523
GSM24664mtDNA "Common"-deletion subject 214.618
GSM24665mtDNA "Common"-deletion subject 32328
GSM24666mtDNA "Common"-deletion subject 46.111