ProfileGDS1065 / 209370_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 77% 72% 68% 68% 60% 68% 64% 81% 56% 76% 81% 80% 75% 69% 68% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1153.177
GSM24653Normal subject 2109.572
GSM24654Normal subject 311868
GSM24655A3243G-MELAS subject 162.368
GSM24656A3243G-MELAS subject 270.860
GSM24657A3243G-MELAS subject 3145.268
GSM24658A3243G-MELAS subject 473.264
GSM24659A3243G-PEO subject 1139.281
GSM24660A3243G-PEO subject 251.656
GSM24661A3243G-PEO subject 39976
GSM24662A3243G-PEO subject 4159.681
GSM24663mtDNA "Common"-deletion subject 1185.580
GSM24664mtDNA "Common"-deletion subject 2236.575
GSM24665mtDNA "Common"-deletion subject 314869
GSM24666mtDNA "Common"-deletion subject 4157.668