ProfileGDS1065 / 213512_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% 21% 22% 19% 22% 36% 15% 20% 20% 25% 26% 35% 15% 21% 22% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 18.419
GSM24653Normal subject 29.421
GSM24654Normal subject 311.422
GSM24655A3243G-MELAS subject 16.619
GSM24656A3243G-MELAS subject 211.722
GSM24657A3243G-MELAS subject 334.136
GSM24658A3243G-MELAS subject 4515
GSM24659A3243G-PEO subject 18.720
GSM24660A3243G-PEO subject 28.820
GSM24661A3243G-PEO subject 38.625
GSM24662A3243G-PEO subject 41226
GSM24663mtDNA "Common"-deletion subject 122.435
GSM24664mtDNA "Common"-deletion subject 210.815
GSM24665mtDNA "Common"-deletion subject 313.521
GSM24666mtDNA "Common"-deletion subject 414.622