Rattus norvegicus leucine-rich repeat LGI family, member 4 (Lgi4), mRN - Nucleotide

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Loss-of-Function Mutations in LGI4, a Secreted Ligand Involved in Schwann Cell Myelination, Are Responsible for Arthrogryposis Multiplex Congenita. [Am J Hum Genet. 2017]
Loss-of-Function Mutations in LGI4, a Secreted Ligand Involved in Schwann Cell Myelination, Are Responsible for Arthrogryposis Multiplex Congenita.
Xue S, Maluenda J, Marguet F, Shboul M, Quevarec L, Bonnard C, Ng AY, Tohari S, Tan TT, Kong MK, et al. Am J Hum Genet. 2017 Apr 6; 100(4):659-665. Epub 2017 Mar 16.
Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium. [Brief Bioinform. 2011]
Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium.
Gaudet P, Livstone MS, Lewis SE, Thomas PD. Brief Bioinform. 2011 Sep; 12(5):449-62. Epub 2011 Aug 27.
Lgi4 promotes the proliferation and differentiation of glial lineage cells throughout the developing peripheral nervous system. [J Neurosci. 2010]
Lgi4 promotes the proliferation and differentiation of glial lineage cells throughout the developing peripheral nervous system.
Nishino J, Saunders TL, Sagane K, Morrison SJ. Version 2. J Neurosci. 2010 Nov 10; 30(45):15228-40.

RefSeq alternative splicing
See 4 reference mRNA sequence splice variants for the Lgi4 gene.
RefSeq protein product
See the reference protein sequence for leucine-rich repeat LGI family member 4 precursor (NP_955793.1).

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Protein sequence from Nucleotide coding region
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Nucleotide