WebA kinesin heavy chain ( KIF5A) mutation in hereditary spastic paraplegia (SPG10) [1]. BACKGROUND: To our knowledge, up to now, only 2 mutations in the KIF5A gene, a … Webkinesin family member 5A: Chromosome: 12: Chromosomal band: q13.13: Imprinted: Unknown: Genomic reference: NG_008155.1: Transcript reference: NM_004984.2: …
KIF5A - en-academic.com
WebKinesin family member 5A (KIF5A), a gene previously linked to two rare neurodegenerative disorders, has been definitively connected to amyotrophic lateral … Webkinesin family member 5A: Calculated molecular weight: 1032 aa, 117 kDa: Observed molecular weight: 118-120 kDa: GenBank accession number: BC146670: Gene symbol: … co to jest bit
Kinesin 5A / KIF5A - LSBio
Kinesin family member 5A is a protein that in humans is encoded by the KIF5A gene. This gene encodes a member of the kinesin family of proteins. Members of this family are part of a multi-subunit complex that functions as a microtubule motor in intracellular organelle transport. Mutations in this gene … Meer weergeven KIF5A has been shown to interact with KLC1. Meer weergeven • Fichera M, Lo Giudice M, Falco M, Sturnio M, Amata S, Calabrese O, et al. (September 2004). "Evidence of kinesin heavy chain (KIF5A) involvement in pure hereditary … Meer weergeven Mutations in KIF5A have been reported to cause hereditary spastic paraplegia type 10 (SPG1). Mutations in … Meer weergeven • Overview of all the structural information available in the PDB for UniProt: Q12840 (Kinesin heavy chain isoform 5A) at the PDBe-KB Meer weergeven Web1 mei 1997 · Multiple Kinesin Family Members Expressed in Teleost Retina and RPE include a Novel C-terminal Kinesin. Author links open overlay panel ... seven of the … Web17 sep. 2024 · A novel KIF5A gene variant causes spastic paraplegia and cerebellar ataxia Ann Clin Transl Neurol. 2024 Sep 17;5 (11):1415-1420. doi: 10.1002/acn3.650. … co to jest bipv