ProfileGDS1065 / 202803_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 67% 67% 59% 63% 62% 65% 70% 72% 66% 69% 70% 61% 65% 65% 61% sort by genotype/variation sort by disease state Gene Expression Profile
Graph caption help
SampleTitleValueRank
GSM24652Normal subject 193.167
GSM24653Normal subject 286.867
GSM24654Normal subject 376.659
GSM24655A3243G-MELAS subject 152.463
GSM24656A3243G-MELAS subject 27662
GSM24657A3243G-MELAS subject 3129.865
GSM24658A3243G-MELAS subject 495.570
GSM24659A3243G-PEO subject 186.272
GSM24660A3243G-PEO subject 278.966
GSM24661A3243G-PEO subject 36969
GSM24662A3243G-PEO subject 485.170
GSM24663mtDNA "Common"-deletion subject 173.361
GSM24664mtDNA "Common"-deletion subject 2145.365
GSM24665mtDNA "Common"-deletion subject 3125.165
GSM24666mtDNA "Common"-deletion subject 4108.461