NINJ1

NINJ1
Identifiers
Aliases	NINJ1, NIN1, NINJURIN, ninjurin 1
External IDs	OMIM: 602062 MGI: 1196617 HomoloGene: 88815 GeneCards: NINJ1
Gene location (Human) Chr. Chromosome 9 (human) Band 9q22.31 Start 93,121,496 bp End 93,134,251 bp
Gene location (Mouse) Chr. Chromosome 13 (mouse) Band 13|13 A5 Start 49,340,961 bp End 49,349,720 bp
RNA expression pattern Bgee Human Mouse (ortholog) Top expressed in left adrenal gland monocyte thoracic aorta ascending aorta right lobe of liver blood gastric mucosa left lobe of thyroid gland right coronary artery skin of abdomen Top expressed in pyloric antrum left lobe of liver facial motor nucleus calvaria utricle secondary oocyte proximal tubule islet of Langerhans kidney parotid gland More reference expression data BioGPS More reference expression data
Gene ontology Molecular function protein binding Cellular component integral component of membrane membrane Biological process hyaloid vascular plexus regression cell adhesion nervous system development tissue regeneration positive regulation of cell-matrix adhesion pyroptosis cell death Sources:Amigo / QuickGO
Orthologs Species Human Mouse Entrez 4814 18081 Ensembl ENSG00000131669 ENSMUSG00000037966 UniProt Q92982 O70131 RefSeq (mRNA) NM_004148 NM_013610 RefSeq (protein) NP_004139 NP_038638 Location (UCSC) Chr 9: 93.12 – 93.13 Mb Chr 13: 49.34 – 49.35 Mb PubMed search
Wikidata
View/Edit Human View/Edit Mouse

Ninjurin-1 is a protein that in humans is encoded by the NINJ1 gene.

Further reading

• Guimarães PE, Fridman C, Gregório SP, et al. (2007). "WITHDRAWN: Association between polymorphisms in genes of inflammatory response and axonal repair with spinal cord injury". Spinal Cord. doi:10.1038/sj.sc.3102122. PMID 17893696.
• Cardoso CC, Martinez AN, Guimarães PE, et al. (2007). "Ninjurin 1 asp110ala single nucleotide polymorphism is associated with protection in leprosy nerve damage". J. Neuroimmunol. 190 (1–2): 131–8. doi:10.1016/j.jneuroim.2007.07.015. PMID 17825431. S2CID 20637695.
• Gerhard DS, Wagner L, Feingold EA, et al. (2004). "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)". Genome Res. 14 (10B): 2121–7. doi:10.1101/gr.2596504. PMC 528928. PMID 15489334.
• Toyama T, Sasaki Y, Horimoto M, et al. (2005). "Ninjurin1 increases p21 expression and induces cellular senescence in human hepatoma cells". J. Hepatol. 41 (4): 637–43. doi:10.1016/j.jhep.2004.06.027. PMID 15464245.
• Humphray SJ, Oliver K, Hunt AR, et al. (2004). "DNA sequence and analysis of human chromosome 9". Nature. 429 (6990): 369–74. Bibcode:2004Natur.429..369H. doi:10.1038/nature02465. PMC 2734081. PMID 15164053.
• Ota T, Suzuki Y, Nishikawa T, et al. (2004). "Complete sequencing and characterization of 21,243 full-length human cDNAs". Nat. Genet. 36 (1): 40–5. doi:10.1038/ng1285. PMID 14702039.
• Strausberg RL, Feingold EA, Grouse LH, et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. Bibcode:2002PNAS...9916899M. doi:10.1073/pnas.242603899. PMC 139241. PMID 12477932.
• Chadwick BP, Heath SK, Williamson J, et al. (1998). "The human homologue of the ninjurin gene maps to the candidate region of hereditary sensory neuropathy type I (HSNI)". Genomics. 47 (1): 58–63. doi:10.1006/geno.1997.5084. PMID 9465296.
• Araki T, Zimonjic DB, Popescu NC, Milbrandt J (1997). "Mechanism of homophilic binding mediated by ninjurin, a novel widely expressed adhesion molecule". J. Biol. Chem. 272 (34): 21373–80. doi:10.1074/jbc.272.34.21373. PMID 9261151.