ProfileGDS1065 / 212483_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 64% 63% 66% 52% 62% 75% 73% 60% 65% 55% 70% 68% 61% 67% 73% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 180.364
GSM24653Normal subject 272.463
GSM24654Normal subject 3109.366
GSM24655A3243G-MELAS subject 134.652
GSM24656A3243G-MELAS subject 275.962
GSM24657A3243G-MELAS subject 3214.475
GSM24658A3243G-MELAS subject 4113.773
GSM24659A3243G-PEO subject 154.560
GSM24660A3243G-PEO subject 274.165
GSM24661A3243G-PEO subject 339.255
GSM24662A3243G-PEO subject 485.570
GSM24663mtDNA "Common"-deletion subject 196.968
GSM24664mtDNA "Common"-deletion subject 2122.661
GSM24665mtDNA "Common"-deletion subject 3133.867
GSM24666mtDNA "Common"-deletion subject 4203.873