Varaico: Literature-Extracted Genetic Variants

Gene:TLR4
Variant:p.E474K
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TLR4

NM_138554.5:p.E474K

Associated Papers

Genetic variation of the Toll-like receptors in a Swedish allergic rhinitis case population.

Henmyr V et al.

Bmc Medical Genetics, 2017

28228119 (PubMed )
Supplement: 12881_2017_379_MOESM8_ESM.xlsx › TabS4

Novel compound heterozygous mutations in CNGA1in a Chinese family affected with autosomal recessive retinitis pigmentosa by targeted sequencing.

Wang M et al.

Bmc Ophthalmology, 2016

Characterization of Disease-Associated Mutations in Human Transmembrane Proteins.

Molnár J et al.

Plos One, 2016

26986070 (PubMed )
Supplement: pone.0151760.s001.xlsx › polymorphism

Association of TLR4 gene polymorphisms with susceptibility to type 2 diabetes mellitus in the Chinese Han population.

Lei T et al.

International Immunopharmacology, 2015

Genetic polymorphisms of the TLR4 gene and their association with susceptibility to type 2 diabetes mellitus in the Chinese population.

Fu XD et al.

Genetics and Molecular Research : Gmr, 2013

Donor polymorphisms of toll-like receptor 4 associated with graft failure in liver transplant recipients.

Oetting WS et al.

Liver Transplantation : Official Publication of the American Association for the Study of Liver Diseases and the International Liver Transplantation Society, 2012

Genome-wide analysis to predict protein sequence variations that change phosphorylation sites or their corresponding kinases.

Ryu GM et al.

Nucleic Acids Research, 2009

19139070 (PubMed )
Supplement: gkn1008_nar-01723-s-2008-File009.xls › TypeII-

Sequence variants of toll-like receptor 4 are associated with prostate cancer risk: results from the CAncer Prostate in Sweden Study.

Zheng SL et al.

Cancer Research, 2004

Polymorphisms in toll-like receptor 4 are not associated with asthma or atopy-related phenotypes.

Raby BA et al.

American Journal of Respiratory and Critical Care Medicine, 2002

Excess of rare amino acid polymorphisms in the Toll-like receptor 4 in humans.

Smirnova I et al.

Genetics, 2001

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Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."