ProfileGDS1065 / 218196_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% 66% 73% 76% 69% 65% 52% 65% 71% 54% 64% 76% 80% 72% 71% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1114.972
GSM24653Normal subject 282.266
GSM24654Normal subject 3150.373
GSM24655A3243G-MELAS subject 189.976
GSM24656A3243G-MELAS subject 299.769
GSM24657A3243G-MELAS subject 3128.365
GSM24658A3243G-MELAS subject 443.752
GSM24659A3243G-PEO subject 166.765
GSM24660A3243G-PEO subject 297.971
GSM24661A3243G-PEO subject 336.654
GSM24662A3243G-PEO subject 466.264
GSM24663mtDNA "Common"-deletion subject 1151.676
GSM24664mtDNA "Common"-deletion subject 2326.580
GSM24665mtDNA "Common"-deletion subject 3174.672
GSM24666mtDNA "Common"-deletion subject 4180.871