ProfileGDS1065 / 210891_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 96% 96% 95% 95% 96% 97% 96% 96% 96% 95% 97% 95% 95% 95% 96% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 11208.996
GSM24653Normal subject 21025.696
GSM24654Normal subject 31125.295
GSM24655A3243G-MELAS subject 1547.895
GSM24656A3243G-MELAS subject 21109.296
GSM24657A3243G-MELAS subject 32360.497
GSM24658A3243G-MELAS subject 41232.296
GSM24659A3243G-PEO subject 1789.396
GSM24660A3243G-PEO subject 2881.496
GSM24661A3243G-PEO subject 3648.395
GSM24662A3243G-PEO subject 41181.997
GSM24663mtDNA "Common"-deletion subject 1101995
GSM24664mtDNA "Common"-deletion subject 21441.395
GSM24665mtDNA "Common"-deletion subject 31585.295
GSM24666mtDNA "Common"-deletion subject 4231896