ProfileGDS1065 / 220370_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 33% 15% 36% 34% 13% 29% 42% 9% 29% 18% 14% 20% 4% 18% 34% sort by genotype/variation sort by disease state Gene Expression Profile
Graph caption help
SampleTitleValueRank
GSM24652Normal subject 120.233
GSM24653Normal subject 25.815
GSM24654Normal subject 327.936
GSM24655A3243G-MELAS subject 116.734
GSM24656A3243G-MELAS subject 26.413
GSM24657A3243G-MELAS subject 322.429
GSM24658A3243G-MELAS subject 428.242
GSM24659A3243G-PEO subject 149
GSM24660A3243G-PEO subject 215.129
GSM24661A3243G-PEO subject 35.518
GSM24662A3243G-PEO subject 45.214
GSM24663mtDNA "Common"-deletion subject 18.920
GSM24664mtDNA "Common"-deletion subject 24.24
GSM24665mtDNA "Common"-deletion subject 311.418
GSM24666mtDNA "Common"-deletion subject 430.934