ProfileGDS1065 / 209103_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 93% 88% 90% 86% 90% 92% 91% 93% 91% 92% 91% 91% 88% 92% 90% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1640.993
GSM24653Normal subject 2318.288
GSM24654Normal subject 3512.590
GSM24655A3243G-MELAS subject 1170.686
GSM24656A3243G-MELAS subject 2388.590
GSM24657A3243G-MELAS subject 3923.292
GSM24658A3243G-MELAS subject 4428.391
GSM24659A3243G-PEO subject 1382.893
GSM24660A3243G-PEO subject 238091
GSM24661A3243G-PEO subject 3360.892
GSM24662A3243G-PEO subject 4371.791
GSM24663mtDNA "Common"-deletion subject 1508.591
GSM24664mtDNA "Common"-deletion subject 2604.988
GSM24665mtDNA "Common"-deletion subject 3839.992
GSM24666mtDNA "Common"-deletion subject 4789.390