ProfileGDS1065 / 205160_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 52% 68% 59% 60% 61% 63% 52% 49% 43% 56% 57% 59% 71% 55% 65% sort by genotype/variation sort by disease state Gene Expression Profile
Graph caption help
SampleTitleValueRank
GSM24652Normal subject 148.552
GSM24653Normal subject 290.968
GSM24654Normal subject 377.259
GSM24655A3243G-MELAS subject 145.960
GSM24656A3243G-MELAS subject 271.961
GSM24657A3243G-MELAS subject 3115.963
GSM24658A3243G-MELAS subject 442.752
GSM24659A3243G-PEO subject 136.449
GSM24660A3243G-PEO subject 231.343
GSM24661A3243G-PEO subject 340.756
GSM24662A3243G-PEO subject 449.157
GSM24663mtDNA "Common"-deletion subject 165.159
GSM24664mtDNA "Common"-deletion subject 2195.371
GSM24665mtDNA "Common"-deletion subject 381.955
GSM24666mtDNA "Common"-deletion subject 413665