ProfileGDS1065 / 220466_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 44% 35% 44% 56% 42% 50% 38% 63% 42% 58% 53% 37% 42% 46% 40% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 13444
GSM24653Normal subject 222.535
GSM24654Normal subject 340.244
GSM24655A3243G-MELAS subject 139.856
GSM24656A3243G-MELAS subject 234.542
GSM24657A3243G-MELAS subject 362.950
GSM24658A3243G-MELAS subject 423.238
GSM24659A3243G-PEO subject 160.363
GSM24660A3243G-PEO subject 230.442
GSM24661A3243G-PEO subject 344.158
GSM24662A3243G-PEO subject 44353
GSM24663mtDNA "Common"-deletion subject 125.437
GSM24664mtDNA "Common"-deletion subject 257.642
GSM24665mtDNA "Common"-deletion subject 355.846
GSM24666mtDNA "Common"-deletion subject 443.640