ProfileGDS1065 / 222093_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 48% 32% 37% 36% 35% 50% 44% 38% 43% 38% 34% 40% 26% 57% 39% sort by genotype/variation sort by disease state Gene Expression Profile
Graph caption help
SampleTitleValueRank
GSM24652Normal subject 14148
GSM24653Normal subject 218.732
GSM24654Normal subject 329.437
GSM24655A3243G-MELAS subject 118.336
GSM24656A3243G-MELAS subject 224.535
GSM24657A3243G-MELAS subject 364.850
GSM24658A3243G-MELAS subject 429.944
GSM24659A3243G-PEO subject 123.238
GSM24660A3243G-PEO subject 230.943
GSM24661A3243G-PEO subject 318.538
GSM24662A3243G-PEO subject 418.734
GSM24663mtDNA "Common"-deletion subject 128.640
GSM24664mtDNA "Common"-deletion subject 225.426
GSM24665mtDNA "Common"-deletion subject 387.857
GSM24666mtDNA "Common"-deletion subject 440.139