ProfileGDS1065 / 217691_x_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 86% 78% 79% 76% 85% 83% 86% 88% 86% 87% 88% 88% 72% 81% 74% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 1293.986
GSM24653Normal subject 2150.478
GSM24654Normal subject 3211.979
GSM24655A3243G-MELAS subject 192.876
GSM24656A3243G-MELAS subject 2253.985
GSM24657A3243G-MELAS subject 3356.183
GSM24658A3243G-MELAS subject 4258.186
GSM24659A3243G-PEO subject 1218.288
GSM24660A3243G-PEO subject 2230.186
GSM24661A3243G-PEO subject 3197.387
GSM24662A3243G-PEO subject 4279.388
GSM24663mtDNA "Common"-deletion subject 1334.588
GSM24664mtDNA "Common"-deletion subject 2204.372
GSM24665mtDNA "Common"-deletion subject 3294.481
GSM24666mtDNA "Common"-deletion subject 421374