LOXL4

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

Lysyl oxidase homolog 4 is an enzyme that in humans is encoded by the LOXL4 gene.[5][6]

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LOXL4
Identifiers
AliasesLOXL4, LOXC, lysyl oxidase like 4
External IDsOMIM: 607318; MGI: 1914823; HomoloGene: 12977; GeneCards: LOXL4; OMA:LOXL4 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_032211

NM_001164311
NM_053083

RefSeq (protein)

NP_115587

NP_001157783
NP_444313

Location (UCSC)Chr 10: 98.25 – 98.27 MbChr 19: 42.58 – 42.6 Mb
PubMed search[3][4]
Wikidata
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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.[6]

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