ProfileGDS1065 / 210830_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 56% 45% 63% 42% 47% 43% 45% 38% 43% 11% 13% 34% 54% 64% 60% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 157.156
GSM24653Normal subject 235.245
GSM24654Normal subject 392.863
GSM24655A3243G-MELAS subject 123.942
GSM24656A3243G-MELAS subject 241.647
GSM24657A3243G-MELAS subject 347.943
GSM24658A3243G-MELAS subject 431.445
GSM24659A3243G-PEO subject 123.638
GSM24660A3243G-PEO subject 231.243
GSM24661A3243G-PEO subject 33.511
GSM24662A3243G-PEO subject 44.613
GSM24663mtDNA "Common"-deletion subject 121.134
GSM24664mtDNA "Common"-deletion subject 292.854
GSM24665mtDNA "Common"-deletion subject 3117.164
GSM24666mtDNA "Common"-deletion subject 4103.660