ProfileGDS1065 / 222383_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 6% 13% 9% 6% 11% 6% 11% 3% 5% 5% 7% 13% 8% 5% 5% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 136
GSM24653Normal subject 25.313
GSM24654Normal subject 34.19
GSM24655A3243G-MELAS subject 12.46
GSM24656A3243G-MELAS subject 25.411
GSM24657A3243G-MELAS subject 33.86
GSM24658A3243G-MELAS subject 43.811
GSM24659A3243G-PEO subject 11.93
GSM24660A3243G-PEO subject 22.65
GSM24661A3243G-PEO subject 31.95
GSM24662A3243G-PEO subject 42.87
GSM24663mtDNA "Common"-deletion subject 15.513
GSM24664mtDNA "Common"-deletion subject 268
GSM24665mtDNA "Common"-deletion subject 33.55
GSM24666mtDNA "Common"-deletion subject 43.35