ProfileGDS1065 / 210653_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 40% 41% 60% 35% 54% 31% 24% 19% 47% 32% 19% 47% 54% 49% 42% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 129.240
GSM24653Normal subject 229.641
GSM24654Normal subject 382.960
GSM24655A3243G-MELAS subject 117.135
GSM24656A3243G-MELAS subject 254.454
GSM24657A3243G-MELAS subject 326.231
GSM24658A3243G-MELAS subject 49.924
GSM24659A3243G-PEO subject 18.319
GSM24660A3243G-PEO subject 237.347
GSM24661A3243G-PEO subject 313.432
GSM24662A3243G-PEO subject 47.219
GSM24663mtDNA "Common"-deletion subject 14147
GSM24664mtDNA "Common"-deletion subject 291.554
GSM24665mtDNA "Common"-deletion subject 361.449
GSM24666mtDNA "Common"-deletion subject 445.942