ProfileGDS1065 / 209378_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 51% 68% 72% 70% 58% 54% 66% 64% 62% 58% 64% 71% 59% 73% 63% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 14751
GSM24653Normal subject 28868
GSM24654Normal subject 3143.672
GSM24655A3243G-MELAS subject 168.470
GSM24656A3243G-MELAS subject 265.158
GSM24657A3243G-MELAS subject 376.154
GSM24658A3243G-MELAS subject 478.366
GSM24659A3243G-PEO subject 16464
GSM24660A3243G-PEO subject 266.662
GSM24661A3243G-PEO subject 34358
GSM24662A3243G-PEO subject 46564
GSM24663mtDNA "Common"-deletion subject 1112.971
GSM24664mtDNA "Common"-deletion subject 2115.459
GSM24665mtDNA "Common"-deletion subject 318673
GSM24666mtDNA "Common"-deletion subject 4121.763