ProfileGDS1065 / 221953_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 58% 61% 40% 45% 30% 45% 67% 31% 50% 59% 61% 33% 21% 27% 27% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 160.958
GSM24653Normal subject 266.961
GSM24654Normal subject 333.940
GSM24655A3243G-MELAS subject 126.945
GSM24656A3243G-MELAS subject 219.530
GSM24657A3243G-MELAS subject 350.845
GSM24658A3243G-MELAS subject 482.367
GSM24659A3243G-PEO subject 116.931
GSM24660A3243G-PEO subject 24250
GSM24661A3243G-PEO subject 34659
GSM24662A3243G-PEO subject 457.361
GSM24663mtDNA "Common"-deletion subject 120.533
GSM24664mtDNA "Common"-deletion subject 217.121
GSM24665mtDNA "Common"-deletion subject 32127
GSM24666mtDNA "Common"-deletion subject 421.227