ProfileGDS1065 / 203230_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 95% 96% 92% 93% 95% 96% 94% 96% 96% 96% 96% 95% 93% 93% 94% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1983.895
GSM24653Normal subject 2955.396
GSM24654Normal subject 373992
GSM24655A3243G-MELAS subject 137193
GSM24656A3243G-MELAS subject 2830.195
GSM24657A3243G-MELAS subject 31684.596
GSM24658A3243G-MELAS subject 4644.994
GSM24659A3243G-PEO subject 1734.796
GSM24660A3243G-PEO subject 2930.696
GSM24661A3243G-PEO subject 3837.296
GSM24662A3243G-PEO subject 41061.396
GSM24663mtDNA "Common"-deletion subject 11040.595
GSM24664mtDNA "Common"-deletion subject 2992.193
GSM24665mtDNA "Common"-deletion subject 3985.693
GSM24666mtDNA "Common"-deletion subject 41359.494