ProfileGDS1065 / 213736_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 52% 54% 22% 61% 54% 80% 44% 80% 77% 88% 90% 32% 18% 25% 50% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 148.252
GSM24653Normal subject 250.654
GSM24654Normal subject 311.222
GSM24655A3243G-MELAS subject 149.161
GSM24656A3243G-MELAS subject 254.854
GSM24657A3243G-MELAS subject 3296.180
GSM24658A3243G-MELAS subject 430.744
GSM24659A3243G-PEO subject 1128.380
GSM24660A3243G-PEO subject 2131.977
GSM24661A3243G-PEO subject 321288
GSM24662A3243G-PEO subject 4312.190
GSM24663mtDNA "Common"-deletion subject 119.132
GSM24664mtDNA "Common"-deletion subject 213.818
GSM24665mtDNA "Common"-deletion subject 318.925
GSM24666mtDNA "Common"-deletion subject 465.550