ProfileGDS1065 / 205414_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% 34% 40% 19% 30% 42% 45% 34% 32% 29% 33% 38% 30% 32% 38% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 120.133
GSM24653Normal subject 221.734
GSM24654Normal subject 333.540
GSM24655A3243G-MELAS subject 16.919
GSM24656A3243G-MELAS subject 219.430
GSM24657A3243G-MELAS subject 344.742
GSM24658A3243G-MELAS subject 432.445
GSM24659A3243G-PEO subject 11934
GSM24660A3243G-PEO subject 218.532
GSM24661A3243G-PEO subject 311.429
GSM24662A3243G-PEO subject 41833
GSM24663mtDNA "Common"-deletion subject 126.838
GSM24664mtDNA "Common"-deletion subject 232.130
GSM24665mtDNA "Common"-deletion subject 328.232
GSM24666mtDNA "Common"-deletion subject 439.338