Homo sapiens choline transporter-like protein 2 isoform 2 (SLC44A2) ge - Nucleotide

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SLC44A2 regulates vascular smooth muscle cell phenotypic switching and aortic aneurysm. [J Clin Invest. 2024]
SLC44A2 regulates vascular smooth muscle cell phenotypic switching and aortic aneurysm.
Song T, Zhao S, Luo S, Chen C, Liu X, Wu X, Sun Z, Cao J, Wang Z, Wang Y, et al. J Clin Invest. 2024 Jun 25; 134(16). Epub 2024 Jun 25.
Lack of the human choline transporter-like protein SLC44A2 causes hearing impairment and a rare red blood phenotype. [EMBO Mol Med. 2023]
Lack of the human choline transporter-like protein SLC44A2 causes hearing impairment and a rare red blood phenotype.
Koehl B, Vrignaud C, Mikdar M, Nair TS, Yang L, Landry S, Laiguillon G, Giroux-Lathuile C, Anselme-Martin S, El Kenz H, et al. EMBO Mol Med. 2023 Mar 8; 15(3):e16320. Epub 2023 Jan 25.
TRIM67 drives tumorigenesis in oligodendrogliomas through Rho GTPase-dependent membrane blebbing. [Neuro Oncol. 2023]
TRIM67 drives tumorigenesis in oligodendrogliomas through Rho GTPase-dependent membrane blebbing.
Demirdizen E, Al-Ali R, Narayanan A, Sun X, Varga JP, Steffl B, Brom M, Krunic D, Schmidt C, Schmidt G, et al. Neuro Oncol. 2023 Jun 2; 25(6):1031-1043.

RefSeq alternative splicing
See 8 reference mRNA sequence splice variants for the SLC44A2 gene.

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Nucleotide