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
Taxonomy sequences associated with Nucleotide record
Annotated Genomic
Genomic sequence records that have the current RNA records as annotated features marking the exons of genes.
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Functional Class
Functional class of the sequence domain architecture
Gene
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OMIM
OMIM records associated with Nucleotide sequence
PubMed (RefSeq)
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PubMed (Weighted)
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GenScript latest version of gene cDNA ORF Clone [GenScript latest version of g...]
GenScript latest version of gene cDNA ORF Clone
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