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PKD1L2 gene

Known as: KIAA1879, PKD1L2, PC1L2 
National Institutes of Health

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2 relations
PKD1 genePKD2L1 gene

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
A four-mRNA model to improve the prediction of breast cancer prognosis.
2019
2019
Genetic basis for plasma amino acid concentrations based on absolute quantification: a genome-wide association study in the Japanese population
To assess the use of plasma free amino acids (PFAAs) as biomarkers for metabolic disorders, it is essential to identify genetic… 
2018
2018
Author Correction: Whole exome sequencing reveals rare variants linked to congenital pouch colon
A correction to this article has been published and is linked from the HTML and PDF versions of this paper. The error has been… 
2018
2018
Whole exome sequencing reveals rare variants linked to congenital pouch colon
We demonstrate the application of whole exome sequencing to discover the rare variants for congenital pouch colon, acronymed CPC… 
2017
2017
A copy number variation in PKD1L2 is associated with colorectal cancer predisposition in korean population
Recently reported genome‐wide association studies have identified more than 20 common low‐penetrance colorectal cancer (CRC… 
2016
2016
Genetic Modifiers of White Blood Cell Count, Albuminuria and Glomerular Filtration Rate in Children with Sickle Cell Anemia
Discovery and validation of genetic variants that influence disease severity in children with sickle cell anemia (SCA) could lead… 
2014
2014
The TRPP subfamily and polycystin-1 proteins.
It has been exciting times since the identification of polycystic kidney disease 1 (PKD1) and PKD2 as the genes mutated in… 
2009
2009
Upregulation of PKD1L2 provokes a complex neuromuscular disease in the mouse
Following a screen for neuromuscular mouse mutants, we identified ostes, a novel N-ethyl N-nitrosourea-induced mouse mutant with… 
2009
2009
The TRPP Channel PKD1L2 Is Linked with a Complex Neuromuscular Disease in the Mouse
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