ProfileGDS1065 / 220582_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 41% 36% 36% 51% 29% 23% 32% 26% 38% 29% 25% 36% 35% 28% 32% sort by genotype/variation sort by disease state Gene Expression Profile
Graph caption help
SampleTitleValueRank
GSM24652Normal subject 13141
GSM24653Normal subject 223.136
GSM24654Normal subject 327.436
GSM24655A3243G-MELAS subject 134.251
GSM24656A3243G-MELAS subject 217.829
GSM24657A3243G-MELAS subject 314.923
GSM24658A3243G-MELAS subject 416.632
GSM24659A3243G-PEO subject 112.926
GSM24660A3243G-PEO subject 225.538
GSM24661A3243G-PEO subject 311.529
GSM24662A3243G-PEO subject 411.225
GSM24663mtDNA "Common"-deletion subject 124.236
GSM24664mtDNA "Common"-deletion subject 242.535
GSM24665mtDNA "Common"-deletion subject 323.128
GSM24666mtDNA "Common"-deletion subject 427.732