ProfileGDS1065 / 213378_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 68% 62% 60% 72% 70% 60% 61% 63% 69% 72% 62% 65% 68% 67% 64% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 195.968
GSM24653Normal subject 267.662
GSM24654Normal subject 380.960
GSM24655A3243G-MELAS subject 175.272
GSM24656A3243G-MELAS subject 2103.370
GSM24657A3243G-MELAS subject 310160
GSM24658A3243G-MELAS subject 464.561
GSM24659A3243G-PEO subject 160.863
GSM24660A3243G-PEO subject 287.169
GSM24661A3243G-PEO subject 378.472
GSM24662A3243G-PEO subject 460.262
GSM24663mtDNA "Common"-deletion subject 185.965
GSM24664mtDNA "Common"-deletion subject 216968
GSM24665mtDNA "Common"-deletion subject 3137.167
GSM24666mtDNA "Common"-deletion subject 4127.564