ProfileGDS1065 / 209334_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 60% 63% 61% 59% 60% 56% 55% 65% 64% 66% 55% 64% 57% 64% 61% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 167.560
GSM24653Normal subject 271.463
GSM24654Normal subject 386.961
GSM24655A3243G-MELAS subject 144.859
GSM24656A3243G-MELAS subject 26960
GSM24657A3243G-MELAS subject 383.556
GSM24658A3243G-MELAS subject 447.855
GSM24659A3243G-PEO subject 164.665
GSM24660A3243G-PEO subject 270.464
GSM24661A3243G-PEO subject 359.166
GSM24662A3243G-PEO subject 445.855
GSM24663mtDNA "Common"-deletion subject 181.964
GSM24664mtDNA "Common"-deletion subject 2103.257
GSM24665mtDNA "Common"-deletion subject 3119.364
GSM24666mtDNA "Common"-deletion subject 4110.461