Homo sapiens kinesin family member 1A (KIF1A), transcript variant 9, m - Nucleotide

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Autosomal dominant neurodevelopmental disorders associated with KIF1A gene variants in 6 pediatric patients. [Zhejiang Da Xue Xue Bao Yi Xue...]
Autosomal dominant neurodevelopmental disorders associated with KIF1A gene variants in 6 pediatric patients.
Lin J, Li N, Yao R, Yu T, Wang X, Wang J. Zhejiang Da Xue Xue Bao Yi Xue Ban. 2023 Dec 12; 52(6):693-700. Epub 2023 Dec 12.
Antagonistic roles of canonical and Alternative-RPA in disease-associated tandem CAG repeat instability. [Cell. 2023]
Antagonistic roles of canonical and Alternative-RPA in disease-associated tandem CAG repeat instability.
Gall-Duncan T, Luo J, Jurkovic CM, Fischer LA, Fujita K, Deshmukh AL, Harding RJ, Tran S, Mehkary M, Li V, et al. Cell. 2023 Oct 26; 186(22):4898-4919.e25. Epub 2023 Oct 11.
[KIF1A gene-associated neurological disease: the correlation between genotype and phenotype]. [Rev Neurol. 2023]
[KIF1A gene-associated neurological disease: the correlation between genotype and phenotype].
Ortiz-Ortigosa A, Calvo-Medina R, Ruiz-García C, Vera-Medialdea R, Ramos-Fernández JM. Rev Neurol. 2023 Sep 16; 77(6):141-145.

RefSeq protein product
See the reference protein sequence for kinesin-like protein KIF1A isoform 9 (NP_001366563.1).

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Protein sequence from Nucleotide coding region
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Nucleotide