ProfileGDS1065 / 203837_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 65% 71% 65% 67% 72% 74% 65% 66% 63% 68% 74% 67% 63% 70% 70% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 181.965
GSM24653Normal subject 210271
GSM24654Normal subject 3100.465
GSM24655A3243G-MELAS subject 160.367
GSM24656A3243G-MELAS subject 2115.472
GSM24657A3243G-MELAS subject 3196.774
GSM24658A3243G-MELAS subject 47565
GSM24659A3243G-PEO subject 166.966
GSM24660A3243G-PEO subject 267.763
GSM24661A3243G-PEO subject 364.868
GSM24662A3243G-PEO subject 4107.574
GSM24663mtDNA "Common"-deletion subject 194.967
GSM24664mtDNA "Common"-deletion subject 2137.263
GSM24665mtDNA "Common"-deletion subject 3157.370
GSM24666mtDNA "Common"-deletion subject 4171.870