ProfileGDS1065 / 211299_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 24% 13% 40% 36% 37% 14% 38% 18% 33% 37% 19% 12% 38% 29% 23% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 112.224
GSM24653Normal subject 25.213
GSM24654Normal subject 333.140
GSM24655A3243G-MELAS subject 118.236
GSM24656A3243G-MELAS subject 22737
GSM24657A3243G-MELAS subject 37.314
GSM24658A3243G-MELAS subject 423.738
GSM24659A3243G-PEO subject 17.618
GSM24660A3243G-PEO subject 219.133
GSM24661A3243G-PEO subject 317.937
GSM24662A3243G-PEO subject 47.119
GSM24663mtDNA "Common"-deletion subject 1512
GSM24664mtDNA "Common"-deletion subject 24738
GSM24665mtDNA "Common"-deletion subject 32429
GSM24666mtDNA "Common"-deletion subject 416.123