ProfileGDS1065 / 201068_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 97% 97% 96% 97% 96% 97% 96% 96% 96% 96% 96% 96% 97% 96% 97% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 11572.697
GSM24653Normal subject 21684.897
GSM24654Normal subject 31708.596
GSM24655A3243G-MELAS subject 1846.497
GSM24656A3243G-MELAS subject 2983.796
GSM24657A3243G-MELAS subject 3271197
GSM24658A3243G-MELAS subject 41077.196
GSM24659A3243G-PEO subject 1714.496
GSM24660A3243G-PEO subject 21022.396
GSM24661A3243G-PEO subject 3874.996
GSM24662A3243G-PEO subject 4952.896
GSM24663mtDNA "Common"-deletion subject 11309.996
GSM24664mtDNA "Common"-deletion subject 22396.697
GSM24665mtDNA "Common"-deletion subject 32136.396
GSM24666mtDNA "Common"-deletion subject 42553.497