ProfileGDS1065 / 219434_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 26% 36% 36% 31% 38% 30% 18% 47% 35% 41% 47% 43% 28% 6% 29% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 113.926
GSM24653Normal subject 22336
GSM24654Normal subject 328.136
GSM24655A3243G-MELAS subject 114.531
GSM24656A3243G-MELAS subject 229.338
GSM24657A3243G-MELAS subject 32430
GSM24658A3243G-MELAS subject 46.318
GSM24659A3243G-PEO subject 13447
GSM24660A3243G-PEO subject 221.635
GSM24661A3243G-PEO subject 321.441
GSM24662A3243G-PEO subject 432.847
GSM24663mtDNA "Common"-deletion subject 134.343
GSM24664mtDNA "Common"-deletion subject 22828
GSM24665mtDNA "Common"-deletion subject 34.16
GSM24666mtDNA "Common"-deletion subject 423.229