ProfileGDS1065 / 203474_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 36% 45% 42% 54% 31% 41% 46% 40% 30% 41% 43% 44% 52% 39% 38% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 123.636
GSM24653Normal subject 234.945
GSM24654Normal subject 337.342
GSM24655A3243G-MELAS subject 137.554
GSM24656A3243G-MELAS subject 220.231
GSM24657A3243G-MELAS subject 343.741
GSM24658A3243G-MELAS subject 433.446
GSM24659A3243G-PEO subject 125.740
GSM24660A3243G-PEO subject 216.130
GSM24661A3243G-PEO subject 321.541
GSM24662A3243G-PEO subject 428.143
GSM24663mtDNA "Common"-deletion subject 134.744
GSM24664mtDNA "Common"-deletion subject 284.652
GSM24665mtDNA "Common"-deletion subject 341.139
GSM24666mtDNA "Common"-deletion subject 438.438