Homo sapiens kinesin family member 5A (KIF5A), transcript variant 1, m - Nucleotide

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Whole-Genome Sequencing Identified a Novel Mutation in the N-Terminal Domain of KIF5A in Chinese Patients with Familial Amyotrophic Lateral Sclerosis. [Genes (Basel). 2024]
Whole-Genome Sequencing Identified a Novel Mutation in the N-Terminal Domain of KIF5A in Chinese Patients with Familial Amyotrophic Lateral Sclerosis.
Wang H, Guan L, Ma X, Wang Y, Wang J, Zhang P, Deng M. Genes (Basel). 2024 May 24; 15(6). Epub 2024 May 24.
A multiscale approach reveals the molecular architecture of the autoinhibited kinesin KIF5A. [J Biol Chem. 2024]
A multiscale approach reveals the molecular architecture of the autoinhibited kinesin KIF5A.
Carrington G, Fatima U, Caramujo I, Lewis T, Casas-Mao D, Peckham M. J Biol Chem. 2024 Mar; 300(3):105713. Epub 2024 Feb 1.
ALS-Associated KIF5A Mutation Causes Locomotor Deficits Associated with Cytoplasmic Inclusions, Alterations of Neuromuscular Junctions, and Motor Neuron Loss. [J Neurosci. 2023]
ALS-Associated KIF5A Mutation Causes Locomotor Deficits Associated with Cytoplasmic Inclusions, Alterations of Neuromuscular Junctions, and Motor Neuron Loss.
Soustelle L, Aimond F, López-Andrés C, Brugioti V, Raoul C, Layalle S. J Neurosci. 2023 Nov 22; 43(47):8058-8072. Epub 2023 Nov 22.

RefSeq alternative splicing
See the other reference mRNA sequence splice variant for the KIF5A gene (NM_001354705.2).
RefSeq protein product
See the reference protein sequence for kinesin heavy chain isoform 5A isoform 1 (NP_004975.2).

Protein
Protein sequence from Nucleotide coding region
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Nucleotide