ProfileGDS1065 / 207323_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 59% 67% 70% 61% 61% 53% 64% 68% 61% 56% 51% 62% 64% 62% 53% sort by genotype/variation sort by disease state Gene Expression Profile
Graph caption help
SampleTitleValueRank
GSM24652Normal subject 164.259
GSM24653Normal subject 284.467
GSM24654Normal subject 313170
GSM24655A3243G-MELAS subject 148.761
GSM24656A3243G-MELAS subject 271.361
GSM24657A3243G-MELAS subject 373.553
GSM24658A3243G-MELAS subject 473.864
GSM24659A3243G-PEO subject 173.968
GSM24660A3243G-PEO subject 26461
GSM24661A3243G-PEO subject 340.456
GSM24662A3243G-PEO subject 438.451
GSM24663mtDNA "Common"-deletion subject 174.462
GSM24664mtDNA "Common"-deletion subject 2142.664
GSM24665mtDNA "Common"-deletion subject 3108.862
GSM24666mtDNA "Common"-deletion subject 475.453