ProfileGDS1065 / 207761_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 95% 96% 95% 97% 96% 96% 96% 96% 97% 96% 96% 94% 95% 95% 98% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 11024.495
GSM24653Normal subject 21091.996
GSM24654Normal subject 31111.795
GSM24655A3243G-MELAS subject 1108897
GSM24656A3243G-MELAS subject 21016.796
GSM24657A3243G-MELAS subject 31849.696
GSM24658A3243G-MELAS subject 41287.796
GSM24659A3243G-PEO subject 1790.396
GSM24660A3243G-PEO subject 21438.397
GSM24661A3243G-PEO subject 3721.796
GSM24662A3243G-PEO subject 41064.196
GSM24663mtDNA "Common"-deletion subject 1729.194
GSM24664mtDNA "Common"-deletion subject 21588.895
GSM24665mtDNA "Common"-deletion subject 31425.195
GSM24666mtDNA "Common"-deletion subject 43614.798