IFNA6
From Wikipedia, the free encyclopedia
Interferon, alpha 6
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Identifiers | ||||||||||||||
Symbol(s) | IFNA6; | |||||||||||||
External IDs | OMIM: 147566 HomoloGene: 86118 | |||||||||||||
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RNA expression pattern | ||||||||||||||
Orthologs | ||||||||||||||
Human | Mouse | |||||||||||||
Entrez | 3443 | n/a | ||||||||||||
Ensembl | ENSG00000120235 | n/a | ||||||||||||
Uniprot | P05013 | n/a | ||||||||||||
Refseq | NM_021002 (mRNA) NP_066282 (protein) |
n/a (mRNA) n/a (protein) |
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Location | Chr 9: 21.34 - 21.34 Mb | n/a | ||||||||||||
Pubmed search | [1] | n/a |
Interferon, alpha 6, also known as IFNA6, is a human gene.[1]
[edit] References
[edit] Further reading
- 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: . PMID 15489334.
- Zhang Z, Henzel WJ (2005). "Signal peptide prediction based on analysis of experimentally verified cleavage sites.". Protein Sci. 13 (10): 2819–24. doi: . PMID 15340161.
- Hardy MP, Owczarek CM, Jermiin LS, et al. (2005). "Characterization of the type I interferon locus and identification of novel genes.". Genomics 84 (2): 331–45. doi: . PMID 15233997.
- 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: . PMID 12477932.
- Nyman TA, Tölö H, Parkkinen J, Kalkkinen N (1998). "Identification of nine interferon-alpha subtypes produced by Sendai virus-induced human peripheral blood leucocytes.". Biochem. J. 329 ( Pt 2): 295–302. PMID 9425112.
- Tiefenbrun N, Melamed D, Levy N, et al. (1996). "Alpha interferon suppresses the cyclin D3 and cdc25A genes, leading to a reversible G0-like arrest.". Mol. Cell. Biol. 16 (7): 3934–44. PMID 8668211.
- Henco K, Brosius J, Fujisawa A, et al. (1985). "Structural relationship of human interferon alpha genes and pseudogenes.". J. Mol. Biol. 185 (2): 227–60. PMID 4057246.
- Olopade OI, Bohlander SK, Pomykala H, et al. (1992). "Mapping of the shortest region of overlap of deletions of the short arm of chromosome 9 associated with human neoplasia.". Genomics 14 (2): 437–43. PMID 1385305.