ProfileGDS1065 / 204207_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 67% 70% 60% 61% 70% 57% 63% 67% 66% 60% 28% 63% 69% 69% 64% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 192.767
GSM24653Normal subject 29970
GSM24654Normal subject 381.760
GSM24655A3243G-MELAS subject 147.861
GSM24656A3243G-MELAS subject 2102.970
GSM24657A3243G-MELAS subject 386.757
GSM24658A3243G-MELAS subject 468.963
GSM24659A3243G-PEO subject 171.267
GSM24660A3243G-PEO subject 277.666
GSM24661A3243G-PEO subject 347.560
GSM24662A3243G-PEO subject 413.128
GSM24663mtDNA "Common"-deletion subject 178.763
GSM24664mtDNA "Common"-deletion subject 2179.469
GSM24665mtDNA "Common"-deletion subject 3149.969
GSM24666mtDNA "Common"-deletion subject 4123.464