ProfileGDS1065 / 210134_x_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 9% 37% 23% 17% 3% 22% 11% 4% 11% 22% 8% 30% 15% 8% 27% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 13.99
GSM24653Normal subject 22437
GSM24654Normal subject 312.523
GSM24655A3243G-MELAS subject 1617
GSM24656A3243G-MELAS subject 22.13
GSM24657A3243G-MELAS subject 314.222
GSM24658A3243G-MELAS subject 43.711
GSM24659A3243G-PEO subject 12.34
GSM24660A3243G-PEO subject 24.711
GSM24661A3243G-PEO subject 37.122
GSM24662A3243G-PEO subject 43.18
GSM24663mtDNA "Common"-deletion subject 116.930
GSM24664mtDNA "Common"-deletion subject 211.515
GSM24665mtDNA "Common"-deletion subject 358
GSM24666mtDNA "Common"-deletion subject 420.827