ProfileGDS1065 / 215141_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 39% 36% 23% 41% 34% 35% 43% 32% 39% 41% 47% 49% 35% 27% 28% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 127.639
GSM24653Normal subject 223.136
GSM24654Normal subject 31223
GSM24655A3243G-MELAS subject 12341
GSM24656A3243G-MELAS subject 224.434
GSM24657A3243G-MELAS subject 331.635
GSM24658A3243G-MELAS subject 429.543
GSM24659A3243G-PEO subject 117.532
GSM24660A3243G-PEO subject 226.339
GSM24661A3243G-PEO subject 321.541
GSM24662A3243G-PEO subject 433.147
GSM24663mtDNA "Common"-deletion subject 144.349
GSM24664mtDNA "Common"-deletion subject 240.635
GSM24665mtDNA "Common"-deletion subject 320.727
GSM24666mtDNA "Common"-deletion subject 422.228