ProfileGDS1065 / 209325_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 54% 59% 52% 40% 55% 24% 51% 44% 55% 36% 25% 61% 49% 56% 57% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 152.954
GSM24653Normal subject 261.559
GSM24654Normal subject 357.752
GSM24655A3243G-MELAS subject 122.240
GSM24656A3243G-MELAS subject 257.455
GSM24657A3243G-MELAS subject 316.624
GSM24658A3243G-MELAS subject 441.451
GSM24659A3243G-PEO subject 129.644
GSM24660A3243G-PEO subject 250.955
GSM24661A3243G-PEO subject 31736
GSM24662A3243G-PEO subject 41125
GSM24663mtDNA "Common"-deletion subject 172.861
GSM24664mtDNA "Common"-deletion subject 274.649
GSM24665mtDNA "Common"-deletion subject 384.456
GSM24666mtDNA "Common"-deletion subject 489.257