ProfileGDS1065 / 219275_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 77% 78% 80% 76% 75% 79% 80% 66% 75% 68% 71% 75% 81% 83% 80% sort by genotype/variation sort by disease state Gene Expression Profile
Graph caption help
SampleTitleValueRank
GSM24652Normal subject 1158.877
GSM24653Normal subject 2146.378
GSM24654Normal subject 3230.580
GSM24655A3243G-MELAS subject 189.276
GSM24656A3243G-MELAS subject 213175
GSM24657A3243G-MELAS subject 3269.479
GSM24658A3243G-MELAS subject 4173.880
GSM24659A3243G-PEO subject 167.666
GSM24660A3243G-PEO subject 2119.875
GSM24661A3243G-PEO subject 364.768
GSM24662A3243G-PEO subject 488.371
GSM24663mtDNA "Common"-deletion subject 1136.575
GSM24664mtDNA "Common"-deletion subject 2344.881
GSM24665mtDNA "Common"-deletion subject 334283
GSM24666mtDNA "Common"-deletion subject 4309.480