ProfileGDS1065 / 204775_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% 22% 55% 17% 44% 55% 41% 18% 63% 18% 41% 41% 47% 58% 70% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 146.551
GSM24653Normal subject 21022
GSM24654Normal subject 367.155
GSM24655A3243G-MELAS subject 15.917
GSM24656A3243G-MELAS subject 238.144
GSM24657A3243G-MELAS subject 380.355
GSM24658A3243G-MELAS subject 426.341
GSM24659A3243G-PEO subject 17.818
GSM24660A3243G-PEO subject 267.763
GSM24661A3243G-PEO subject 35.618
GSM24662A3243G-PEO subject 426.241
GSM24663mtDNA "Common"-deletion subject 130.641
GSM24664mtDNA "Common"-deletion subject 269.447
GSM24665mtDNA "Common"-deletion subject 389.258
GSM24666mtDNA "Common"-deletion subject 4172.470