ProfileGDS1065 / 211198_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 14% 11% 6% 8% 13% 6% 11% 9% 6% 24% 6% 9% 7% 6% 9% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 15.614
GSM24653Normal subject 24.611
GSM24654Normal subject 33.36
GSM24655A3243G-MELAS subject 138
GSM24656A3243G-MELAS subject 26.413
GSM24657A3243G-MELAS subject 33.86
GSM24658A3243G-MELAS subject 43.711
GSM24659A3243G-PEO subject 14.29
GSM24660A3243G-PEO subject 22.86
GSM24661A3243G-PEO subject 38.424
GSM24662A3243G-PEO subject 42.56
GSM24663mtDNA "Common"-deletion subject 149
GSM24664mtDNA "Common"-deletion subject 25.77
GSM24665mtDNA "Common"-deletion subject 34.26
GSM24666mtDNA "Common"-deletion subject 44.89