ProfileGDS1065 / 210252_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 82% 76% 73% 72% 74% 76% 83% 78% 73% 79% 80% 77% 75% 75% 78% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1215.282
GSM24653Normal subject 2133.276
GSM24654Normal subject 3151.873
GSM24655A3243G-MELAS subject 176.172
GSM24656A3243G-MELAS subject 2130.574
GSM24657A3243G-MELAS subject 3222.876
GSM24658A3243G-MELAS subject 4205.983
GSM24659A3243G-PEO subject 1115.178
GSM24660A3243G-PEO subject 2107.173
GSM24661A3243G-PEO subject 3119.179
GSM24662A3243G-PEO subject 4143.780
GSM24663mtDNA "Common"-deletion subject 1157.777
GSM24664mtDNA "Common"-deletion subject 2241.975
GSM24665mtDNA "Common"-deletion subject 3207.975
GSM24666mtDNA "Common"-deletion subject 4267.978