ProfileGDS1065 / 219563_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 81% 81% 80% 82% 71% 85% 80% 82% 75% 84% 80% 77% 77% 70% 81% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1192.881
GSM24653Normal subject 2186.181
GSM24654Normal subject 3225.180
GSM24655A3243G-MELAS subject 1129.482
GSM24656A3243G-MELAS subject 2111.871
GSM24657A3243G-MELAS subject 3406.585
GSM24658A3243G-MELAS subject 4174.180
GSM24659A3243G-PEO subject 1144.282
GSM24660A3243G-PEO subject 2115.375
GSM24661A3243G-PEO subject 3159.184
GSM24662A3243G-PEO subject 4151.480
GSM24663mtDNA "Common"-deletion subject 1153.377
GSM24664mtDNA "Common"-deletion subject 2270.177
GSM24665mtDNA "Common"-deletion subject 3154.870
GSM24666mtDNA "Common"-deletion subject 4337.981