ProfileGDS1065 / 200624_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 91% 93% 96% 92% 95% 93% 95% 90% 92% 84% 89% 93% 96% 95% 96% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1489.791
GSM24653Normal subject 2604.493
GSM24654Normal subject 3137996
GSM24655A3243G-MELAS subject 1327.692
GSM24656A3243G-MELAS subject 2794.795
GSM24657A3243G-MELAS subject 31022.693
GSM24658A3243G-MELAS subject 4822.895
GSM24659A3243G-PEO subject 1292.790
GSM24660A3243G-PEO subject 2452.992
GSM24661A3243G-PEO subject 3159.584
GSM24662A3243G-PEO subject 4297.989
GSM24663mtDNA "Common"-deletion subject 1625.393
GSM24664mtDNA "Common"-deletion subject 21793.396
GSM24665mtDNA "Common"-deletion subject 31603.395
GSM24666mtDNA "Common"-deletion subject 41790.796