Mus musculus ALX homeobox 1 (Alx1), transcript variant 1, mRNA

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Loss of Neogenin alters branchial arch development and leads to craniofacial skeletal defects. [Front Cell Dev Biol. 2024]
Loss of Neogenin alters branchial arch development and leads to craniofacial skeletal defects.
Quilez S, Dumontier E, Baim C, Kam J, Cloutier JF. Front Cell Dev Biol. 2024; 12:1256465. Epub 2024 Feb 9.
TFAP2 paralogs regulate midfacial development in part through a conserved ALX genetic pathway. [Development. 2024]
TFAP2 paralogs regulate midfacial development in part through a conserved ALX genetic pathway.
Nguyen TT, Mitchell JM, Kiel MD, Kenny CP, Li H, Jones KL, Cornell RA, Williams TJ, Nichols JT, Van Otterloo E. Development. 2024 Jan 1; 151(1). Epub 2024 Jan 2.
Three-dimensional molecular architecture of mouse organogenesis. [Nat Commun. 2023]
Three-dimensional molecular architecture of mouse organogenesis.
Qu F, Li W, Xu J, Zhang R, Ke J, Ren X, Meng X, Qin L, Zhang J, Lu F, et al. Nat Commun. 2023 Jul 31; 14(1):4599. Epub 2023 Jul 31.

RefSeq alternative splicing
See 5 reference mRNA sequence splice variants for the Alx1 gene.
RefSeq protein product
See the reference protein sequence for ALX homeobox protein 1 isoform 1 (NP_766141.1).

Protein
Protein sequence from Nucleotide coding region
PubMed
PubMed articles cited by Nucleotide sequence record
Taxonomy
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Genomic sequence records that have the current RNA records as annotated features marking the exons of genes.
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Functional Class
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OMIM
OMIM records associated with Nucleotide sequence
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Nucleotide