PREDICTED: Mus musculus SPNS lysolipid transporter 1, lysophospholipid - Nucleotide

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Lack of SPNS1 results in accumulation of lysolipids and lysosomal storage disease in mouse models. [JCI Insight. 2024]
Lack of SPNS1 results in accumulation of lysolipids and lysosomal storage disease in mouse models.
Ha HT, Liu S, Nguyen XT, Vo LK, Leong NC, Nguyen DT, Balamurugan S, Lim PY, Wu Y, Seong E, et al. JCI Insight. 2024 Mar 7; 9(8). Epub 2024 Mar 7.
Genetic determinants of micronucleus formation in vivo. [Nature. 2024]
Genetic determinants of micronucleus formation in vivo.
Adams DJ, Barlas B, McIntyre RE, Salguero I, van der Weyden L, Barros A, Vicente JR, Karimpour N, Haider A, Ranzani M, et al. Nature. 2024 Mar; 627(8002):130-136. Epub 2024 Feb 14.
Spns1 is a lysophospholipid transporter mediating lysosomal phospholipid salvage. [Proc Natl Acad Sci U S A. 2022]
Spns1 is a lysophospholipid transporter mediating lysosomal phospholipid salvage.
He M, Kuk ACY, Ding M, Chin CF, Galam DLA, Nah JM, Tan BC, Yeo HL, Chua GL, Benke PI, et al. Proc Natl Acad Sci U S A. 2022 Oct 4; 119(40):e2210353119. Epub 2022 Sep 26.

RefSeq alternative splicing
See the other reference mRNA sequence splice variant for the Spns1 gene (NM_023712.3).
RefSeq protein product
See the reference protein sequence for protein spinster homolog 1 isoform X1 (XP_036009367.1).

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Nucleotide