ProfileGDS1065 / 201344_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 65% 68% 64% 67% 67% 69% 67% 69% 66% 71% 69% 65% 67% 62% 66% sort by genotype/variation sort by disease state Gene Expression Profile
Graph caption help
SampleTitleValueRank
GSM24652Normal subject 184.265
GSM24653Normal subject 287.968
GSM24654Normal subject 399.264
GSM24655A3243G-MELAS subject 160.567
GSM24656A3243G-MELAS subject 289.767
GSM24657A3243G-MELAS subject 3155.869
GSM24658A3243G-MELAS subject 481.867
GSM24659A3243G-PEO subject 178.169
GSM24660A3243G-PEO subject 279.566
GSM24661A3243G-PEO subject 374.171
GSM24662A3243G-PEO subject 482.769
GSM24663mtDNA "Common"-deletion subject 186.765
GSM24664mtDNA "Common"-deletion subject 2157.767
GSM24665mtDNA "Common"-deletion subject 3105.462
GSM24666mtDNA "Common"-deletion subject 4139.366