Harmonizome 3.0

kinesin light chain 2

The protein encoded by this gene is a light chain of kinesin, a molecular motor responsible for moving vesicles and organelles along microtubules. Defects in this gene are a cause of spastic paraplegia, optic atrophy, and neuropathy (SPOAN) syndrome. [provided by RefSeq, Mar 2016]

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term klc2 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

From NURSA Protein-Protein Interactions

interacting proteins for KLC2 from the NURSA Protein-Protein Interactions dataset.

From Pathway Commons Protein-Protein Interactions

interacting proteins for KLC2 from the Pathway Commons Protein-Protein Interactions dataset.

From CM4AI KOLF21J CRISPRi Gene Perturbation Atlas

genes differentially expressed following the KLC2 gene perturbation from the CM4AI KOLF21J CRISPRi Gene Perturbation Atlas.

From CORUM Protein Complexes

proteins in the uKHC-KLC1-KLC2 kinesin complex protein complex from the CORUM Protein Complexes dataset.

From CORUM Protein Complexes

proteins in the KLC2-nKHC-uKHC kinesin complex protein complex from the CORUM Protein Complexes dataset.

From CORUM Protein Complexes

proteins in the nKHC-KLC1-KLC2 kinesin complex protein complex from the CORUM Protein Complexes dataset.