ProfileGDS1065 / 214718_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% 56% 58% 54% 57% 56% 60% 53% 48% 52% 45% 56% 65% 44% 69% sort by genotype/variation sort by disease state Gene Expression Profile
Graph caption help
SampleTitleValueRank
GSM24652Normal subject 147.752
GSM24653Normal subject 254.156
GSM24654Normal subject 37658
GSM24655A3243G-MELAS subject 13754
GSM24656A3243G-MELAS subject 26157
GSM24657A3243G-MELAS subject 384.856
GSM24658A3243G-MELAS subject 460.960
GSM24659A3243G-PEO subject 141.753
GSM24660A3243G-PEO subject 23948
GSM24661A3243G-PEO subject 33452
GSM24662A3243G-PEO subject 430.345
GSM24663mtDNA "Common"-deletion subject 158.156
GSM24664mtDNA "Common"-deletion subject 2146.765
GSM24665mtDNA "Common"-deletion subject 351.444
GSM24666mtDNA "Common"-deletion subject 4160.569