ProfileGDS1065 / 202112_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 96% 96% 93% 97% 95% 97% 96% 96% 96% 96% 96% 96% 97% 94% 94% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 11445.796
GSM24653Normal subject 21263.596
GSM24654Normal subject 3842.993
GSM24655A3243G-MELAS subject 1819.597
GSM24656A3243G-MELAS subject 2939.195
GSM24657A3243G-MELAS subject 32218.297
GSM24658A3243G-MELAS subject 4124396
GSM24659A3243G-PEO subject 1901.196
GSM24660A3243G-PEO subject 21103.896
GSM24661A3243G-PEO subject 3713.296
GSM24662A3243G-PEO subject 41099.896
GSM24663mtDNA "Common"-deletion subject 11212.396
GSM24664mtDNA "Common"-deletion subject 22296.397
GSM24665mtDNA "Common"-deletion subject 31292.694
GSM24666mtDNA "Common"-deletion subject 41336.194