ProfileGDS1065 / 219972_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 33% 29% 37% 33% 44% 41% 37% 36% 33% 37% 35% 27% 40% 43% 50% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 120.333
GSM24653Normal subject 215.829
GSM24654Normal subject 329.637
GSM24655A3243G-MELAS subject 116.133
GSM24656A3243G-MELAS subject 237.344
GSM24657A3243G-MELAS subject 343.541
GSM24658A3243G-MELAS subject 421.837
GSM24659A3243G-PEO subject 121.236
GSM24660A3243G-PEO subject 219.133
GSM24661A3243G-PEO subject 317.937
GSM24662A3243G-PEO subject 420.135
GSM24663mtDNA "Common"-deletion subject 114.327
GSM24664mtDNA "Common"-deletion subject 252.240
GSM24665mtDNA "Common"-deletion subject 349.243
GSM24666mtDNA "Common"-deletion subject 465.750