ProfileGDS1065 / 221939_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 65% 46% 61% 44% 25% 68% 56% 48% 68% 79% 74% 63% 64% 63% 62% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 185.165
GSM24653Normal subject 236.546
GSM24654Normal subject 38661
GSM24655A3243G-MELAS subject 125.744
GSM24656A3243G-MELAS subject 214.325
GSM24657A3243G-MELAS subject 3145.668
GSM24658A3243G-MELAS subject 451.156
GSM24659A3243G-PEO subject 134.848
GSM24660A3243G-PEO subject 283.268
GSM24661A3243G-PEO subject 3117.979
GSM24662A3243G-PEO subject 4106.174
GSM24663mtDNA "Common"-deletion subject 179.463
GSM24664mtDNA "Common"-deletion subject 2139.764
GSM24665mtDNA "Common"-deletion subject 3112.563
GSM24666mtDNA "Common"-deletion subject 4113.962