NINJ1

From Wikipedia, the free encyclopedia

Ninjurin 1

Identifiers

NINJ1; NIN1; NINJURIN

External IDs

OMIM: 602062 HomoloGene: 88702

Gene ontology
Molecular Function:	• protein binding
Cellular Component:	• membrane • integral to membrane
Biological Process:	• cell adhesion • nervous system development • tissue regeneration

RNA expression pattern

More reference expression data

Orthologs

Human

Mouse

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Refseq

NM_004148 (mRNA)
NP_004139 (protein)

n/a (mRNA)
n/a (protein)

Location

Chr 9: 94.92 - 94.94 Mb

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Pubmed search

[1]

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Ninjurin 1, also known as NINJ1, is a human gene.^[1]

[edit] References

^ Entrez Gene: NINJ1 ninjurin 1.

[edit] Further reading

Guimarães PE, Fridman C, Gregório SP, et al.. "WITHDRAWN: Association between polymorphisms in genes of inflammatory response and axonal repair with spinal cord injury.". 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.
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. 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. doi:10.1038/nature02465. 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. doi:10.1073/pnas.242603899. 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. PMID 9261151.
Araki T, Milbrandt J (1996). "Ninjurin, a novel adhesion molecule, is induced by nerve injury and promotes axonal growth.". Neuron 17 (2): 353-61. PMID 8780658.