plexin-D1 isoform X2 [Homo sapiens]

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Poland-Möbius syndrome: a case report implicating a novel mutation of the PLXND1 gene and literature review. [BMC Pediatr. 2022]
Poland-Möbius syndrome: a case report implicating a novel mutation of the PLXND1 gene and literature review.
Glass GE, Mohammedali S, Sivakumar B, Stotland MA, Abdulkader F, Prosser DO, Love DR. BMC Pediatr. 2022 Dec 30; 22(1):745. Epub 2022 Dec 30.
Biallelic alterations in PLXND1 cause common arterial trunk and other cardiac malformations in humans. [Hum Mol Genet. 2023]
Biallelic alterations in PLXND1 cause common arterial trunk and other cardiac malformations in humans.
Guimier A, de Pontual L, Braddock SR, Torti E, Pérez-Jurado LA, Muñoz-Cabello P, Arumí M, Monaghan KG, Lee H, Wang LK, et al. Hum Mol Genet. 2023 Jan 13; 32(3):353-356.
Identification of plexin D1 on circulating extracellular vesicles as a potential biomarker of polymyositis and dermatomyositis. [Rheumatology (Oxford). 2022]
Identification of plexin D1 on circulating extracellular vesicles as a potential biomarker of polymyositis and dermatomyositis.
Uto K, Ueda K, Okano T, Akashi K, Takahashi S, Nakamachi Y, Imanishi T, Awano H, Morinobu A, Kawano S, et al. Rheumatology (Oxford). 2022 Apr 11; 61(4):1669-1679.

RefSeq mRNA
See reference mRNA sequence for the PLXND1 gene (XM_011512589.2).
RefSeq protein isoforms
See 13 reference sequence protein isoforms for the PLXND1 gene.

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Protein