ProfileGDS1065 / 215181_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 19% 39% 54% 20% 57% 22% 50% 41% 57% 31% 61% 39% 44% 34% 40% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 18.319
GSM24653Normal subject 226.439
GSM24654Normal subject 362.354
GSM24655A3243G-MELAS subject 1720
GSM24656A3243G-MELAS subject 261.957
GSM24657A3243G-MELAS subject 313.522
GSM24658A3243G-MELAS subject 440.250
GSM24659A3243G-PEO subject 126.641
GSM24660A3243G-PEO subject 254.757
GSM24661A3243G-PEO subject 312.831
GSM24662A3243G-PEO subject 45961
GSM24663mtDNA "Common"-deletion subject 128.139
GSM24664mtDNA "Common"-deletion subject 262.744
GSM24665mtDNA "Common"-deletion subject 331.134
GSM24666mtDNA "Common"-deletion subject 443.140