ProfileGDS1065 / 209537_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 77% 76% 81% 83% 78% 74% 76% 86% 82% 76% 78% 77% 74% 79% 77% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1152.277
GSM24653Normal subject 2134.276
GSM24654Normal subject 323781
GSM24655A3243G-MELAS subject 1132.183
GSM24656A3243G-MELAS subject 2161.278
GSM24657A3243G-MELAS subject 3198.974
GSM24658A3243G-MELAS subject 4132.776
GSM24659A3243G-PEO subject 1190.186
GSM24660A3243G-PEO subject 2176.982
GSM24661A3243G-PEO subject 39576
GSM24662A3243G-PEO subject 4129.678
GSM24663mtDNA "Common"-deletion subject 1159.377
GSM24664mtDNA "Common"-deletion subject 2232.174
GSM24665mtDNA "Common"-deletion subject 3261.979
GSM24666mtDNA "Common"-deletion subject 4261.777