ProfileGDS1065 / 216716_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 8% 13% 30% 18% 4% 9% 7% 14% 24% 32% 21% 21% 32% 31% 9% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 13.58
GSM24653Normal subject 25.213
GSM24654Normal subject 32030
GSM24655A3243G-MELAS subject 16.518
GSM24656A3243G-MELAS subject 22.84
GSM24657A3243G-MELAS subject 34.89
GSM24658A3243G-MELAS subject 42.67
GSM24659A3243G-PEO subject 15.914
GSM24660A3243G-PEO subject 211.324
GSM24661A3243G-PEO subject 313.132
GSM24662A3243G-PEO subject 47.921
GSM24663mtDNA "Common"-deletion subject 19.321
GSM24664mtDNA "Common"-deletion subject 23632
GSM24665mtDNA "Common"-deletion subject 327.431
GSM24666mtDNA "Common"-deletion subject 44.99