Homo sapiens LDL receptor related protein 4 (LRP4), mRNA

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LRP4 site-specific variants in the third β-propeller domain causes congenital myasthenic syndrome type 17. [Eur J Med Genet. 2024]
LRP4 site-specific variants in the third β-propeller domain causes congenital myasthenic syndrome type 17.
Al Jabry T, Al-Hashmi N, Abdelhadi B, Al-Maawali A. Eur J Med Genet. 2024 Feb; 67:104903. Epub 2023 Dec 13.
LRP4-related signalling pathways and their regulatory role in neurological diseases. [Brain Res. 2024]
LRP4-related signalling pathways and their regulatory role in neurological diseases.
Chen BH, Lin ZY, Zeng XX, Jiang YH, Geng F. Brain Res. 2024 Feb 15; 1825:148705. Epub 2023 Dec 6.
LRP4 mutations, dental anomalies, and oral exostoses. [Int J Paediatr Dent. 2024]
LRP4 mutations, dental anomalies, and oral exostoses.
Kantaputra P, Panichkul W, Sillapasorn P, Adisornkanj P, Kitsadayurach P, Kaewgaya M, Intachai W, Olsen B, Ngamphiw C, Leethanakul C, et al. Int J Paediatr Dent. 2024 Jul; 34(4):432-441. Epub 2023 Nov 27.

RefSeq alternative splicing
See 7 reference mRNA sequence splice variants for the LRP4 gene.
RefSeq protein product
See the reference protein sequence for low-density lipoprotein receptor-related protein 4 precursor (NP_002325.2).

Protein
Protein sequence from Nucleotide coding region
PubMed
PubMed articles cited by Nucleotide sequence record
Taxonomy
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Annotated Genomic
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Nucleotide