ProfileGDS1065 / 208980_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 98% 98% 99% 98% 99% 98% 98% 98% 98% 98% 98% 98% 98% 99% 98% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 13147.698
GSM24653Normal subject 22527.998
GSM24654Normal subject 35165.199
GSM24655A3243G-MELAS subject 11354.998
GSM24656A3243G-MELAS subject 23971.699
GSM24657A3243G-MELAS subject 34064.598
GSM24658A3243G-MELAS subject 43454.398
GSM24659A3243G-PEO subject 12288.198
GSM24660A3243G-PEO subject 22839.698
GSM24661A3243G-PEO subject 3167598
GSM24662A3243G-PEO subject 42560.498
GSM24663mtDNA "Common"-deletion subject 12627.898
GSM24664mtDNA "Common"-deletion subject 24932.798
GSM24665mtDNA "Common"-deletion subject 36013.599
GSM24666mtDNA "Common"-deletion subject 45246.198