ProfileGDS1065 / 203663_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 99% 99% 99% 99% 99% 99% 99% 99% 99% 99% 99% 99% 99% 99% 99% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 15271.299
GSM24653Normal subject 24966.499
GSM24654Normal subject 3513799
GSM24655A3243G-MELAS subject 12921.499
GSM24656A3243G-MELAS subject 23841.899
GSM24657A3243G-MELAS subject 36268.399
GSM24658A3243G-MELAS subject 44702.599
GSM24659A3243G-PEO subject 14183.899
GSM24660A3243G-PEO subject 23904.999
GSM24661A3243G-PEO subject 34050.199
GSM24662A3243G-PEO subject 45062.899
GSM24663mtDNA "Common"-deletion subject 15662.699
GSM24664mtDNA "Common"-deletion subject 26480.899
GSM24665mtDNA "Common"-deletion subject 35861.499
GSM24666mtDNA "Common"-deletion subject 46909.999