ProfileGDS1065 / 208878_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 65% 66% 66% 67% 72% 68% 62% 69% 71% 73% 76% 73% 74% 73% 72% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 183.165
GSM24653Normal subject 282.166
GSM24654Normal subject 3109.466
GSM24655A3243G-MELAS subject 161.667
GSM24656A3243G-MELAS subject 2115.772
GSM24657A3243G-MELAS subject 3147.668
GSM24658A3243G-MELAS subject 464.862
GSM24659A3243G-PEO subject 175.369
GSM24660A3243G-PEO subject 297.871
GSM24661A3243G-PEO subject 381.773
GSM24662A3243G-PEO subject 4116.176
GSM24663mtDNA "Common"-deletion subject 1126.373
GSM24664mtDNA "Common"-deletion subject 2232.974
GSM24665mtDNA "Common"-deletion subject 3178.173
GSM24666mtDNA "Common"-deletion subject 4188.672