IFNK
From Wikipedia, the free encyclopedia
| Interferon, kappa | |||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Identifiers | |||||||||||||
| Symbols | IFNK; RP11-27J8.1 | ||||||||||||
| External IDs | MGI: 2683287 HomoloGene: 36384 GeneCards: IFNK Gene | ||||||||||||
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| Orthologs | |||||||||||||
| Species | Human | Mouse | |||||||||||
| Entrez | 56832 | 387510 | |||||||||||
| Ensembl | ENSG00000147896 | ENSMUSG00000042993 | |||||||||||
| UniProt | Q9P0W0 | Q7TSL0 | |||||||||||
| RefSeq (mRNA) | NM_020124 | NM_199157 | |||||||||||
| RefSeq (protein) | NP_064509 | NP_954608 | |||||||||||
| Location (UCSC) | Chr 9: 27.52 – 27.53 Mb | Chr 4: 35.15 – 35.15 Mb | |||||||||||
| PubMed search | |||||||||||||
Interferon kappa, also known as IFN-kappa, is a protein that in humans is encoded by the IFNK gene.[1][2][3]
Function
IFN-kappa is a member of the type I interferon family. Type I interferons are a group of related glycoproteins that play an important role in host defenses against viral infections. This protein is expressed in keratinocytes and the gene is found on chromosome 9, adjacent to the type I interferon cluster.[1]
References
- ↑ 1.0 1.1 "Entrez Gene: interferon".
- ↑ LaFleur DW, Nardelli B, Tsareva T, Mather D, Feng P, Semenuk M, Taylor K, Buergin M, Chinchilla D, Roshke V, Chen G, Ruben SM, Pitha PM, Coleman TA, Moore PA (October 2001). "Interferon-kappa, a novel type I interferon expressed in human keratinocytes". J. Biol. Chem. 276 (43): 39765–71. doi:10.1074/jbc.M102502200. PMID 11514542.
- ↑ Nardelli B, Zaritskaya L, Semenuk M, Cho YH, LaFleur DW, Shah D, Ullrich S, Girolomoni G, Albanesi C, Moore PA (November 2002). "Regulatory effect of IFN-kappa, a novel type I IFN, on cytokine production by cells of the innate immune system". J. Immunol. 169 (9): 4822–30. PMID 12391192.
Further reading
- Liu C, Batliwalla F, Li W, et al.. "Genome-wide association scan identifies candidate polymorphisms associated with differential response to anti-TNF treatment in rheumatoid arthritis.". Mol. Med. 14 (9-10): 575–81. doi:10.2119/2008-00056.Liu. PMID 18615156.
- DeCarlo CA, Severini A, Edler L, et al. (2010). "IFN-κ, a novel type I IFN, is undetectable in HPV-positive human cervical keratinocytes.". Lab. Invest. 90 (10): 1482–91. doi:10.1038/labinvest.2010.95. PMID 20479716.
- Silva LK, Blanton RE, Parrado AR, et al. (2010). "Dengue hemorrhagic fever is associated with polymorphisms in JAK1.". Eur. J. Hum. Genet. 18 (11): 1221–7. doi:10.1038/ejhg.2010.98. PMC 2950898. PMID 20588308.
- Yang XR, Liang X, Pfeiffer RM, et al. (2010). "Associations of 9p21 variants with cutaneous malignant melanoma, nevi, and pigmentation phenotypes in melanoma-prone families with and without CDKN2A mutations.". Fam. Cancer 9 (4): 625–33. doi:10.1007/s10689-010-9356-3. PMID 20574843.
- Ferreira RC, Pan-Hammarström Q, Graham RR, et al. (2010). "Association of IFIH1 and other autoimmunity risk alleles with selective IgA deficiency.". Nat. Genet. 42 (9): 777–80. doi:10.1038/ng.644. PMID 20694011.
- Laaksovirta H, Peuralinna T, Schymick JC, et al. (2010). "Chromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association study.". Lancet Neurol 9 (10): 978–85. doi:10.1016/S1474-4422(10)70184-8. PMID 20801718.
- Clark HF, Gurney AL, Abaya E, et al. (2003). "The secreted protein discovery initiative (SPDI), a large-scale effort to identify novel human secreted and transmembrane proteins: a bioinformatics assessment.". Genome Res. 13 (10): 2265–70. doi:10.1101/gr.1293003. PMC 403697. PMID 12975309.
- Rincon-Orozco B, Halec G, Rosenberger S, et al. (2009). "Epigenetic silencing of interferon-kappa in human papillomavirus type 16-positive cells.". Cancer Res. 69 (22): 8718–25. doi:10.1158/0008-5472.CAN-09-0550. PMID 19887612.
- 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. PMC 2734081. PMID 15164053.
- Zhang Z, Henzel WJ (2004). "Signal peptide prediction based on analysis of experimentally verified cleavage sites.". Protein Sci. 13 (10): 2819–24. doi:10.1110/ps.04682504. PMC 2286551. PMID 15340161.
- van Es MA, Veldink JH, Saris CG, et al. (2009). "Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis.". Nat. Genet. 41 (10): 1083–7. doi:10.1038/ng.442. PMID 19734901.
- Harley IT, Niewold TB, Stormont RM, et al. (2010). "The role of genetic variation near interferon-kappa in systemic lupus erythematosus.". J. Biomed. Biotechnol. 2010. doi:10.1155/2010/706825. PMID 20706608.
This article incorporates text from the United States National Library of Medicine, which is in the public domain.
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