Homo sapiens neurexin 1 (NRXN1), transcript variant alpha13, mRNA

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Schizophrenia-associated NRXN1 deletions induce developmental-timing- and cell-type-specific vulnerabilities in human brain organoids. [Nat Commun. 2023]
Schizophrenia-associated NRXN1 deletions induce developmental-timing- and cell-type-specific vulnerabilities in human brain organoids.
Sebastian R, Jin K, Pavon N, Bansal R, Potter A, Song Y, Babu J, Gabriel R, Sun Y, Aronow B, et al. Nat Commun. 2023 Jun 24; 14(1):3770. Epub 2023 Jun 24.
Computational Saturation Mutagenesis to Investigate the Effects of Neurexin-1 Mutations on AlphaFold Structure. [Genes (Basel). 2022]
Computational Saturation Mutagenesis to Investigate the Effects of Neurexin-1 Mutations on AlphaFold Structure.
Rhoades R, Henry B, Prichett D, Fang Y, Teng S. Genes (Basel). 2022 Apr 28; 13(5). Epub 2022 Apr 28.
Homozygous exonic and intragenic NRXN1 deletion presenting as either West syndrome or autism spectrum disorder in two siblings. [Clin Neurol Neurosurg. 2022]
Homozygous exonic and intragenic NRXN1 deletion presenting as either West syndrome or autism spectrum disorder in two siblings.
Aksu Uzunhan T, Ayaz A. Clin Neurol Neurosurg. 2022 Mar; 214:107141. Epub 2022 Jan 24.

RefSeq alternative splicing
See 25 reference mRNA sequence splice variants for the NRXN1 gene.
RefSeq protein product
See the reference protein sequence for neurexin-1 isoform alpha13 precursor (NP_001317023.1).

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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OMIM
OMIM records associated with Nucleotide sequence
PubMed (RefSeq)
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PubMed (Weighted)
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UCSC Genome Browser [UCSC Genome Browser]
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