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XB-GENEPAGE-978895
???displayGene.symbol???: twnk
???displayGene.name???: twinkle mtDNA helicase
???displayGene.synonyms???
c10orf2
(
???displayGene.geneFunction??? mitochondrial DNA helicase twinkle Protein Function
![]() ???displayGene.geneInteractants???
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Diseases: Disease Ontology: autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 3
MIM:
PERRAULT SYNDROME 5; PRLTS5
External Links:
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???displayGene.expression??? | Development Stages Embryonic Tissues Adult Tissues | |||||||||||
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