Resolving TYK2 locus genotype-to-phenotype differences in autoimmunity.
Ontology highlight
ABSTRACT: Thousands of genetic variants have been identified, which contribute to the development of complex diseases, but determining how to elucidate their biological consequences for translation into clinical benefit is challenging. Conflicting evidence regarding the functional impact of genetic variants in the tyrosine kinase 2 (TYK2) gene, which is differentially associated with common autoimmune diseases, currently obscures the potential of TYK2 as a therapeutic target. We aimed to resolve this conflict by performing genetic meta-analysis across disorders; subsequent molecular, cellular, in vivo, and structural functional follow-up; and epidemiological studies. Our data revealed a protective homozygous effect that defined a signaling optimum between autoimmunity and immunodeficiency and identi
SUBMITTER: Dendrou CA
PROVIDER: S-EPMC5737835 | biostudies-literature | 2016 Nov
REPOSITORIES: biostudies-literature
ACCESS DATA