ProfileGDS1065 / 204360_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 53% 15% 30% 30% 45% 41% 14% 54% 35% 48% 45% 35% 35% 38% 49% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 150.353
GSM24653Normal subject 26.115
GSM24654Normal subject 319.830
GSM24655A3243G-MELAS subject 113.730
GSM24656A3243G-MELAS subject 239.445
GSM24657A3243G-MELAS subject 343.141
GSM24658A3243G-MELAS subject 44.814
GSM24659A3243G-PEO subject 143.954
GSM24660A3243G-PEO subject 221.535
GSM24661A3243G-PEO subject 329.448
GSM24662A3243G-PEO subject 430.645
GSM24663mtDNA "Common"-deletion subject 122.935
GSM24664mtDNA "Common"-deletion subject 241.135
GSM24665mtDNA "Common"-deletion subject 337.738
GSM24666mtDNA "Common"-deletion subject 463.249