ProfileGDS1065 / 200968_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 72% 75% 73% 74% 69% 77% 85% 71% 66% 68% 75% 73% 66% 74% 69% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1113.572
GSM24653Normal subject 212575
GSM24654Normal subject 315673
GSM24655A3243G-MELAS subject 181.174
GSM24656A3243G-MELAS subject 298.869
GSM24657A3243G-MELAS subject 3238.377
GSM24658A3243G-MELAS subject 4245.385
GSM24659A3243G-PEO subject 182.271
GSM24660A3243G-PEO subject 278.266
GSM24661A3243G-PEO subject 365.768
GSM24662A3243G-PEO subject 4108.375
GSM24663mtDNA "Common"-deletion subject 1122.873
GSM24664mtDNA "Common"-deletion subject 2155.866
GSM24665mtDNA "Common"-deletion subject 3193.974
GSM24666mtDNA "Common"-deletion subject 4161.769