| Name |
|---|
BRKS1 GeneTelopeptide lysyl hydroxylase, bone-specific |
LOXL1 Genelysyl oxidase-like 1 This gene encodes a member of the lysyl oxidase family of proteins. The prototypic member of the family is essential to the biogenesis of connective tissue, encoding an extracellular copper-dependent amine oxidase that catalyzes the first step in the formation of crosslinks in collagen and elastin. The encoded preproprotein is proteolytically processed to generate the mature enzyme. A highly conserved amino acid sequence at the C-terminus end appears to be sufficient for amine oxidase activity, suggesting that each family member may retain this function. The N-terminus is poorly conserved and may impart additional roles in developmental regulation, senescence, tumor suppression, cell growth control, and chemotaxis to each member of the family. Mutations in this gene are associated with exfoliation syndrome. [provided by RefSeq, Jan 2016] |
LOXL2 Genelysyl oxidase-like 2 This gene encodes a member of the lysyl oxidase gene family. The prototypic member of the family is essential to the biogenesis of connective tissue, encoding an extracellular copper-dependent amine oxidase that catalyses the first step in the formation of crosslinks in collagens and elastin. A highly conserved amino acid sequence at the C-terminus end appears to be sufficient for amine oxidase activity, suggesting that each family member may retain this function. The N-terminus is poorly conserved and may impart additional roles in developmental regulation, senescence, tumor suppression, cell growth control, and chemotaxis to each member of the family. [provided by RefSeq, Jul 2008] |
LOXL3 Genelysyl oxidase-like 3 This gene encodes a lysyl oxidase, which likely functions as an amine oxidase and plays a role in the formation of crosslinks in collagens and elastin. Deletion of the related gene in mouse causes neonatal mortality with cleft palate, spine deformity, and defects in collagen organization. A mutation in this gene was found in a family with Stickler syndrome. [provided by RefSeq, Sep 2016] |
LOXL4 Genelysyl oxidase-like 4 This gene encodes a member of the lysyl oxidase gene family. The prototypic member of the family is essential to the biogenesis of connective tissue, encoding an extracellular copper-dependent amine oxidase that catalyses the first step in the formation of crosslinks in collagens and elastin. A highly conserved amino acid sequence at the C-terminus end appears to be sufficient for amine oxidase activity, suggesting that each family member may retain this function. The N-terminus is poorly conserved and may impart additional roles in developmental regulation, senescence, tumor suppression, cell growth control, and chemotaxis to each member of the family. [provided by RefSeq, Jul 2008] |
LOX Genelysyl oxidase This gene encodes a member of the lysyl oxidase family of proteins. Alternative splicing results in multiple transcript variants, at least one of which encodes a preproprotein that is proteolytically processed to generate a regulatory propeptide and the mature enzyme. The copper-dependent amine oxidase activity of this enzyme functions in the crosslinking of collagens and elastin, while the propeptide may play a role in tumor suppression. In addition, defects in this gene have been linked with predisposition to thoracic aortic aneurysms and dissections. [provided by RefSeq, Jul 2016] |
lysyl-trna aminoacylation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the lysyl-trna aminoacylation biological process from the curated GO Biological Process Annotations 2015 dataset. |
lysyl-tRNA aminoacylation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the lysyl-tRNA aminoacylation biological process from the curated GO Biological Process Annotations 2023 dataset. |
lysyl-tRNA aminoacylation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the lysyl-tRNA aminoacylation biological process from the curated GO Biological Process Annotations 2025 dataset. |
alanyl-tyrosyl-prolyl-glycyl-lysyl-phenylalanine Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical alanyl-tyrosyl-prolyl-glycyl-lysyl-phenylalanine from the curated CTD Gene-Chemical Interactions dataset. |
lysyl Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term lysyl in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
Lysyl oxidase, conserved site Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Lysyl oxidase, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Lysyl oxidase Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Lysyl oxidase protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
lysyl hydroxylase 3 deficiency Gene SetFrom OMIM Gene-Disease Associations genes associated with the lysyl hydroxylase 3 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset. |
aminoacylation Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term aminoacylation in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |