ProfileGDS1065 / 217896_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 78% 73% 75% 70% 75% 74% 79% 77% 75% 76% 77% 79% 75% 78% 72% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1164.378
GSM24653Normal subject 2113.973
GSM24654Normal subject 316875
GSM24655A3243G-MELAS subject 168.770
GSM24656A3243G-MELAS subject 2136.375
GSM24657A3243G-MELAS subject 3196.574
GSM24658A3243G-MELAS subject 4156.579
GSM24659A3243G-PEO subject 1111.177
GSM24660A3243G-PEO subject 2114.575
GSM24661A3243G-PEO subject 399.576
GSM24662A3243G-PEO subject 4125.577
GSM24663mtDNA "Common"-deletion subject 1174.579
GSM24664mtDNA "Common"-deletion subject 2234.175
GSM24665mtDNA "Common"-deletion subject 3251.678
GSM24666mtDNA "Common"-deletion subject 4193.472