ProfileGDS1065 / 204887_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 14% 13% 8% 14% 25% 12% 32% 6% 39% 8% 21% 41% 32% 36% 12% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 15.914
GSM24653Normal subject 25.213
GSM24654Normal subject 33.98
GSM24655A3243G-MELAS subject 14.914
GSM24656A3243G-MELAS subject 214.525
GSM24657A3243G-MELAS subject 36.212
GSM24658A3243G-MELAS subject 417.232
GSM24659A3243G-PEO subject 136
GSM24660A3243G-PEO subject 226.339
GSM24661A3243G-PEO subject 32.78
GSM24662A3243G-PEO subject 47.921
GSM24663mtDNA "Common"-deletion subject 13041
GSM24664mtDNA "Common"-deletion subject 236.432
GSM24665mtDNA "Common"-deletion subject 335.736
GSM24666mtDNA "Common"-deletion subject 46.412