ProfileGDS1065 / 220489_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 19% 24% 11% 34% 7% 5% 8% 14% 27% 17% 9% 15% 6% 20% 6% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 18.319
GSM24653Normal subject 211.624
GSM24654Normal subject 3511
GSM24655A3243G-MELAS subject 116.434
GSM24656A3243G-MELAS subject 23.87
GSM24657A3243G-MELAS subject 33.15
GSM24658A3243G-MELAS subject 42.88
GSM24659A3243G-PEO subject 15.914
GSM24660A3243G-PEO subject 213.927
GSM24661A3243G-PEO subject 35.317
GSM24662A3243G-PEO subject 43.29
GSM24663mtDNA "Common"-deletion subject 16.215
GSM24664mtDNA "Common"-deletion subject 25.26
GSM24665mtDNA "Common"-deletion subject 312.720
GSM24666mtDNA "Common"-deletion subject 43.76