ProfileGDS1065 / 207024_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 20% 11% 19% 23% 23% 18% 10% 19% 15% 21% 20% 24% 19% 15% 14% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 19.320
GSM24653Normal subject 24.411
GSM24654Normal subject 39.219
GSM24655A3243G-MELAS subject 18.523
GSM24656A3243G-MELAS subject 212.123
GSM24657A3243G-MELAS subject 310.118
GSM24658A3243G-MELAS subject 43.510
GSM24659A3243G-PEO subject 18.119
GSM24660A3243G-PEO subject 26.315
GSM24661A3243G-PEO subject 36.821
GSM24662A3243G-PEO subject 47.420
GSM24663mtDNA "Common"-deletion subject 111.124
GSM24664mtDNA "Common"-deletion subject 215.619
GSM24665mtDNA "Common"-deletion subject 38.815
GSM24666mtDNA "Common"-deletion subject 47.614