ProfileGDS1065 / 214270_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 10% 14% 46% 14% 35% 25% 30% 33% 37% 11% 33% 13% 41% 37% 25% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 14.110
GSM24653Normal subject 25.614
GSM24654Normal subject 343.846
GSM24655A3243G-MELAS subject 14.914
GSM24656A3243G-MELAS subject 225.535
GSM24657A3243G-MELAS subject 316.925
GSM24658A3243G-MELAS subject 414.630
GSM24659A3243G-PEO subject 118.233
GSM24660A3243G-PEO subject 223.737
GSM24661A3243G-PEO subject 33.411
GSM24662A3243G-PEO subject 417.433
GSM24663mtDNA "Common"-deletion subject 15.513
GSM24664mtDNA "Common"-deletion subject 253.541
GSM24665mtDNA "Common"-deletion subject 335.937
GSM24666mtDNA "Common"-deletion subject 418.425