ProfileGDS1065 / 204224_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% 39% 37% 22% 27% 34% 43% 18% 30% 26% 25% 36% 40% 38% 37% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 120.833
GSM24653Normal subject 226.839
GSM24654Normal subject 328.937
GSM24655A3243G-MELAS subject 18.222
GSM24656A3243G-MELAS subject 216.327
GSM24657A3243G-MELAS subject 329.934
GSM24658A3243G-MELAS subject 429.343
GSM24659A3243G-PEO subject 17.518
GSM24660A3243G-PEO subject 216.730
GSM24661A3243G-PEO subject 39.426
GSM24662A3243G-PEO subject 411.225
GSM24663mtDNA "Common"-deletion subject 123.636
GSM24664mtDNA "Common"-deletion subject 25340
GSM24665mtDNA "Common"-deletion subject 339.238
GSM24666mtDNA "Common"-deletion subject 436.237