ProfileGDS1065 / 207173_x_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 25% 62% 48% 58% 37% 50% 44% 42% 32% 30% 38% 36% 41% 40% 46% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 113.125
GSM24653Normal subject 268.262
GSM24654Normal subject 347.848
GSM24655A3243G-MELAS subject 14358
GSM24656A3243G-MELAS subject 227.637
GSM24657A3243G-MELAS subject 364.150
GSM24658A3243G-MELAS subject 429.944
GSM24659A3243G-PEO subject 12842
GSM24660A3243G-PEO subject 218.532
GSM24661A3243G-PEO subject 311.830
GSM24662A3243G-PEO subject 42338
GSM24663mtDNA "Common"-deletion subject 124.136
GSM24664mtDNA "Common"-deletion subject 253.941
GSM24665mtDNA "Common"-deletion subject 341.940
GSM24666mtDNA "Common"-deletion subject 454.946