ProfileGDS1065 / 210214_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 38% 34% 47% 41% 52% 30% 37% 39% 33% 38% 5% 40% 43% 51% 47% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 126.838
GSM24653Normal subject 221.334
GSM24654Normal subject 345.947
GSM24655A3243G-MELAS subject 122.541
GSM24656A3243G-MELAS subject 251.352
GSM24657A3243G-MELAS subject 324.530
GSM24658A3243G-MELAS subject 422.537
GSM24659A3243G-PEO subject 124.839
GSM24660A3243G-PEO subject 219.333
GSM24661A3243G-PEO subject 318.338
GSM24662A3243G-PEO subject 42.15
GSM24663mtDNA "Common"-deletion subject 129.940
GSM24664mtDNA "Common"-deletion subject 257.943
GSM24665mtDNA "Common"-deletion subject 369.351
GSM24666mtDNA "Common"-deletion subject 45747