Homo sapiens plexin B2 (PLXNB2), transcript variant 16, mRNA

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In vivo interaction screening reveals liver-derived constraints to metastasis. [Nature. 2024]
In vivo interaction screening reveals liver-derived constraints to metastasis.
Borrelli C, Roberts M, Eletto D, Hussherr MD, Fazilaty H, Valenta T, Lafzi A, Kretz JA, Guido Vinzoni E, Karakatsani A, et al. Nature. 2024 Aug; 632(8024):411-418. Epub 2024 Jul 24.
Biallelic variants in Plexin B2 (PLXNB2) cause amelogenesis imperfecta, hearing loss and intellectual disability. [J Med Genet. 2024]
Biallelic variants in Plexin B2 (PLXNB2) cause amelogenesis imperfecta, hearing loss and intellectual disability.
Smith CEL, Laugel-Haushalter V, Hany U, Best S, Taylor RL, Poulter JA, Wortmann SB, Feichtinger RG, Mayr JA, Al Bahlani S, et al. J Med Genet. 2024 Jun 20; 61(7):689-698. Epub 2024 Jun 20.
Colorectal Cancer-Associated Myofibroblasts Exhibit Enhanced Angiogenin Expression and Signaling via the PLXNB2 Receptor. [J Surg Res. 2024]
Colorectal Cancer-Associated Myofibroblasts Exhibit Enhanced Angiogenin Expression and Signaling via the PLXNB2 Receptor.
Hu A, Nussbaum YI, Mitchem J, Yoo J. J Surg Res. 2024 Apr; 296:273-280. Epub 2024 Jan 30.

RefSeq alternative splicing
See 37 reference mRNA sequence splice variants for the PLXNB2 gene.
RefSeq protein product
See the reference protein sequence for plexin-B2 isoform 3 precursor (NP_001363806.1).

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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OMIM
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Nucleotide