syntaxin-binding protein 5-like isoform X3 [Homo sapiens]

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Homozygous mutation of STXBP5L explains an autosomal recessive infantile-onset neurodegenerative disorder. [Hum Mol Genet. 2015]
Homozygous mutation of STXBP5L explains an autosomal recessive infantile-onset neurodegenerative disorder.
Kumar R, Corbett MA, Smith NJ, Jolly LA, Tan C, Keating DJ, Duffield MD, Utsumi T, Moriya K, Smith KR, et al. Hum Mol Genet. 2015 Apr 1; 24(7):2000-10. Epub 2014 Dec 11.
Multiple variants in toll-like receptor 4 gene modulate risk of liver fibrosis in Caucasians with chronic hepatitis C infection. [J Hepatol. 2009]
Multiple variants in toll-like receptor 4 gene modulate risk of liver fibrosis in Caucasians with chronic hepatitis C infection.
Li Y, Chang M, Abar O, Garcia V, Rowland C, Catanese J, Ross D, Broder S, Shiffman M, Cheung R, et al. J Hepatol. 2009 Oct; 51(4):750-7. Epub 2009 Jun 18.
Novel genetic variants linked to prelabor rupture of membranes among Chinese pregnant women. [Placenta. 2023]
Novel genetic variants linked to prelabor rupture of membranes among Chinese pregnant women.
Kan H, Liu H, Mu Y, Li Y, Zhang M, Cao Y, Dong Y, Li Y, Wang K, Li Q, et al. Placenta. 2023 Jun; 137:14-22. Epub 2023 Apr 7.

RefSeq genomic sequence
See the genomic reference sequence for the STXBP5L gene (NG_052890.1).
RefSeq mRNA
See reference mRNA sequence for the STXBP5L gene (XM_017007534.2).

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Protein