ProfileGDS1065 / 207819_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 66% 56% 58% 57% 67% 30% 45% 47% 59% 52% 42% 37% 59% 74% 70% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 185.366
GSM24653Normal subject 254.256
GSM24654Normal subject 375.658
GSM24655A3243G-MELAS subject 141.357
GSM24656A3243G-MELAS subject 291.267
GSM24657A3243G-MELAS subject 323.830
GSM24658A3243G-MELAS subject 431.345
GSM24659A3243G-PEO subject 134.147
GSM24660A3243G-PEO subject 258.859
GSM24661A3243G-PEO subject 334.552
GSM24662A3243G-PEO subject 42742
GSM24663mtDNA "Common"-deletion subject 124.837
GSM24664mtDNA "Common"-deletion subject 2111.759
GSM24665mtDNA "Common"-deletion subject 3192.574
GSM24666mtDNA "Common"-deletion subject 4176.470