activin A receptor type II-like 1, isoform CRA_c [Homo sapiens]

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Impact of heterozygous ALK1 mutations on the transcriptomic response to BMP9 and BMP10 in endothelial cells from hereditary hemorrhagic telangiectasia and pulmonary arterial hypertension donors. [Angiogenesis. 2024]
Impact of heterozygous ALK1 mutations on the transcriptomic response to BMP9 and BMP10 in endothelial cells from hereditary hemorrhagic telangiectasia and pulmonary arterial hypertension donors.
Al Tabosh T, Liu H, Koça D, Al Tarrass M, Tu L, Giraud S, Delagrange L, Beaudoin M, Rivière S, Grobost V, et al. Angiogenesis. 2024 May; 27(2):211-227. Epub 2024 Jan 31.
Hereditary hemorrhagic telangiectasia: First demonstration of a founder effect in Italy; the ACVRL1 c.289_294del variant originated in the country of Bergamo 200 years ago. [Mol Genet Genomic Med. 2022]
Hereditary hemorrhagic telangiectasia: First demonstration of a founder effect in Italy; the ACVRL1 c.289_294del variant originated in the country of Bergamo 200 years ago.
Sbalchiero A, Abu Hweij Y, Mazza T, Buscarini E, Scotti C, Pagella F, Manfredi G, Matti E, Spinozzi G, Olivieri C. Mol Genet Genomic Med. 2022 Aug; 10(8):e1972. Epub 2022 May 27.
Founder Effects in Hereditary Hemorrhagic Telangiectasia. [J Clin Med. 2021]
Founder Effects in Hereditary Hemorrhagic Telangiectasia.
Major T, Gindele R, Balogh G, Bárdossy P, Bereczky Z. J Clin Med. 2021 Apr 14; 10(8). Epub 2021 Apr 14.

RefSeq genomic sequence
See the genomic reference sequence for the ACVRL1 gene (NG_009549.1).
RefSeq protein isoforms
See 12 reference sequence protein isoforms for the ACVRL1 gene.

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Transcript/Protein Information [PANTHER Classification System]
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reagent reviews [ExactAntigen/Labome]
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reagents [ExactAntigen/Labome]
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